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ROUNDUP WEED KILLER NON-HODGKINS LYMPHOMA CANCER RISK In March 2019, in the first Federal Roundup Weedkiller lawsuit trial, a federal jury awarded $80 million to a man who claimed that his non-Hodgkin’s lymphoma cancer had been caused by use of glyphosate-based Roundup at his job as a landscaper. His case was considered to be a bellwether trial, indicating possible future actionon more than 700
BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
VALSPAR EXTERIOR PAINT PROBLEMS Consumers who painted their homes with Valspar Exterior Paint noticed a number of problems shortly after the paint job was finished. Issues included: Bubbling. Peeling. Expansion. Buckling and warping of the vinyl siding. Valspar has not yet recalled its exterior paint product, but it might still be possible for homeowners to receive CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. ACTEMRA - LIVER FAILURE RISKS - CONSUMER SAFETY GUIDE Actemra, a medication used for the treatment of RA, has been linked to life-threatening side effects including liver failure, cardiovascular events and GI perforation. Genentech, manufacturer of Actemra, may be facing hundreds of lawsuits due to serious complications caused by the medication. People who have suffered liver failure, heart attack BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ROUNDUP WEED KILLER NON-HODGKINS LYMPHOMA CANCER RISK In March 2019, in the first Federal Roundup Weedkiller lawsuit trial, a federal jury awarded $80 million to a man who claimed that his non-Hodgkin’s lymphoma cancer had been caused by use of glyphosate-based Roundup at his job as a landscaper. His case was considered to be a bellwether trial, indicating possible future actionon more than 700
BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
VALSPAR EXTERIOR PAINT PROBLEMS Consumers who painted their homes with Valspar Exterior Paint noticed a number of problems shortly after the paint job was finished. Issues included: Bubbling. Peeling. Expansion. Buckling and warping of the vinyl siding. Valspar has not yet recalled its exterior paint product, but it might still be possible for homeowners to receive CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. CIPRO - AORTIC ANEURYSM OR DISSECTION - CONSUMER SAFETY GUIDE Cipro Aortic Aneurysm or Aortic Dissection. Cipro may interfere with collagen structure which may cause cartilage to become brittle and tear. This is the mechanism by which tendon rupture occurs but may also cause serious cardiac effects that may be deadly. Cipro and other fluoroquinolones weakening of collagen may lead to bulge or rupture in MEDTRONIC MINIMED INSULIN PUMP RECALL LAWSUIT Medtronic Insulin Pump Recall. The FDA issued a safety alert on November 21, 2019, regarding a Class I recall for Medtronic MiniMed Insulin Pump. A Class 1 recall is the highest urgency recall which indicates that the device poses a high risk of serious injury or death. The safety notification stated that Medtronic was recalling thedevices due
MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The ACTEMRA - LIVER FAILURE RISKS - CONSUMER SAFETY GUIDE Actemra, a medication used for the treatment of RA, has been linked to life-threatening side effects including liver failure, cardiovascular events and GI perforation. Genentech, manufacturer of Actemra, may be facing hundreds of lawsuits due to serious complications caused by the medication. People who have suffered liver failure, heart attack PENUMBRA JET 7 XTRA FLEX CATHETER RECALL Penumbra’s Recall of the JET 7 Reperfusion Catheter Due to Distal Tip Damage, U.S. Food and Drug Administration (01/29/2021); Penumbra’s Urgent Voluntary Recall of JET 7 Catheters with Xtra Flex Technology Due to Increased Risk of Mortality and Serious Injury – Urgent Letter to Health Care Providers, U.S. Food and Drug Administration (12/15/2020) WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser TJI Joists with Flak Jacket have been found to be defective and they produce an unpleasant odor. There is also concern the materials used to manufacture the joists contain dangerous chemicals that can cause health complications.POWER MORCELLATORS
Johnson & Johnson under FBI Investigation. Ethicon and Johnson & Johnson suspended the sale of power morcellators shortly after the safety communication was issued. The company stated it had always warned surgeons that the spread of malignant tissue as possible, but because the device was approved via the FDA’s fast track 510 (k)process and
TALCUM POWDER OVARIAN CANCER RISKS Thousands of talcum powder lawsuits have been filed against Johnson & Johnson due to a possible link between talc and ovarian cancer. More than 5,500 women have claimed that J&J’s Shower-to-Shower, Johnson’s Baby Powder and other talc-based powder products TAXOTERE - SIDE EFFECTS AND WARNINGS Taxotere Uses. Taxotere (docetaxel) is an antineoplastic agent used as chemotherapy to treat a number of types of cancer. It is used in combination with other drugs such as cisplatin, fluorouracil, doxorubicin, cyclophosphamide and prednisone and is approved to treat: CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a SCAFFOLDING ACCIDENTS Scaffolding must include toeboards to eliminate the chance for accidentally kicking loose object over the edge. Scaffolds must be at least 10 feet from electric power lines. Scaffolds must be constructed and inspected by trained “competent” personnel. All employees who AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ABILIFY SIDE EFFECT WARNING Bristol-Myers Squibb (BMS), manufacturer of Abilify, has been the subject of thousands of lawsuits. These lawsuits have been filed by Abilify users who claimed that the manufacturer failed to adequately warn them of serious side effects including: Gambling and compulsive behaviors. Stroke. Hyperglycemia and Type 2 diabetes. BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a SCAFFOLDING ACCIDENTS Scaffolding must include toeboards to eliminate the chance for accidentally kicking loose object over the edge. Scaffolds must be at least 10 feet from electric power lines. Scaffolds must be constructed and inspected by trained “competent” personnel. All employees who AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ABILIFY SIDE EFFECT WARNING Bristol-Myers Squibb (BMS), manufacturer of Abilify, has been the subject of thousands of lawsuits. These lawsuits have been filed by Abilify users who claimed that the manufacturer failed to adequately warn them of serious side effects including: Gambling and compulsive behaviors. Stroke. Hyperglycemia and Type 2 diabetes. BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. MEDTRONIC MINIMED INSULIN PUMP RECALL LAWSUIT Medtronic Insulin Pump Recall. The FDA issued a safety alert on November 21, 2019, regarding a Class I recall for Medtronic MiniMed Insulin Pump. A Class 1 recall is the highest urgency recall which indicates that the device poses a high risk of serious injury or death. The safety notification stated that Medtronic was recalling thedevices due
CIPRO - AORTIC ANEURYSM OR DISSECTION - CONSUMER SAFETY GUIDE Cipro Aortic Aneurysm or Aortic Dissection. Cipro may interfere with collagen structure which may cause cartilage to become brittle and tear. This is the mechanism by which tendon rupture occurs but may also cause serious cardiac effects that may be deadly. Cipro and other fluoroquinolones weakening of collagen may lead to bulge or rupture in MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BAIR HUGGER COMPLICATIONS Injuries and Complications Associated with Bair Hugger. Serious complications developed after surgery using the Bair Hugger forced-air warming blanket device have included: Deep joint infections of hip and knee. Antibiotic resistant infections. Sepsis. Need for revision surgery to remove and replace device. ACTEMRA - LIVER FAILURE RISKS - CONSUMER SAFETY GUIDE Actemra, a medication used for the treatment of RA, has been linked to life-threatening side effects including liver failure, cardiovascular events and GI perforation. Genentech, manufacturer of Actemra, may be facing hundreds of lawsuits due to serious complications caused by the medication. People who have suffered liver failure, heart attack PENUMBRA JET 7 XTRA FLEX CATHETER RECALL Penumbra’s Recall of the JET 7 Reperfusion Catheter Due to Distal Tip Damage, U.S. Food and Drug Administration (01/29/2021); Penumbra’s Urgent Voluntary Recall of JET 7 Catheters with Xtra Flex Technology Due to Increased Risk of Mortality and Serious Injury – Urgent Letter to Health Care Providers, U.S. Food and Drug Administration (12/15/2020)POWER MORCELLATORS
Johnson & Johnson under FBI Investigation. Ethicon and Johnson & Johnson suspended the sale of power morcellators shortly after the safety communication was issued. The company stated it had always warned surgeons that the spread of malignant tissue as possible, but because the device was approved via the FDA’s fast track 510 (k)process and
TAXOTERE - SIDE EFFECTS AND WARNINGS - CONSUMER SAFETY GUIDE Taxotere Uses. Taxotere (docetaxel) is an antineoplastic agent used as chemotherapy to treat a number of types of cancer. It is used in combination with other drugs such as cisplatin, fluorouracil, doxorubicin, cyclophosphamide and prednisone and is approved to treat: VALSPAR EXTERIOR PAINT PROBLEMS Consumers who painted their homes with Valspar Exterior Paint noticed a number of problems shortly after the paint job was finished. Issues included: Bubbling. Peeling. Expansion. Buckling and warping of the vinyl siding. Valspar has not yet recalled its exterior paint product, but it might still be possible for homeowners to receive CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a SCAFFOLDING ACCIDENTS Scaffolding must include toeboards to eliminate the chance for accidentally kicking loose object over the edge. Scaffolds must be at least 10 feet from electric power lines. Scaffolds must be constructed and inspected by trained “competent” personnel. All employees who AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ABILIFY SIDE EFFECT WARNING Bristol-Myers Squibb (BMS), manufacturer of Abilify, has been the subject of thousands of lawsuits. These lawsuits have been filed by Abilify users who claimed that the manufacturer failed to adequately warn them of serious side effects including: Gambling and compulsive behaviors. Stroke. Hyperglycemia and Type 2 diabetes. BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a SCAFFOLDING ACCIDENTS Scaffolding must include toeboards to eliminate the chance for accidentally kicking loose object over the edge. Scaffolds must be at least 10 feet from electric power lines. Scaffolds must be constructed and inspected by trained “competent” personnel. All employees who AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ABILIFY SIDE EFFECT WARNING Bristol-Myers Squibb (BMS), manufacturer of Abilify, has been the subject of thousands of lawsuits. These lawsuits have been filed by Abilify users who claimed that the manufacturer failed to adequately warn them of serious side effects including: Gambling and compulsive behaviors. Stroke. Hyperglycemia and Type 2 diabetes. BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. MEDTRONIC MINIMED INSULIN PUMP RECALL LAWSUIT Medtronic Insulin Pump Recall. The FDA issued a safety alert on November 21, 2019, regarding a Class I recall for Medtronic MiniMed Insulin Pump. A Class 1 recall is the highest urgency recall which indicates that the device poses a high risk of serious injury or death. The safety notification stated that Medtronic was recalling thedevices due
CIPRO - AORTIC ANEURYSM OR DISSECTION - CONSUMER SAFETY GUIDE Cipro Aortic Aneurysm or Aortic Dissection. Cipro may interfere with collagen structure which may cause cartilage to become brittle and tear. This is the mechanism by which tendon rupture occurs but may also cause serious cardiac effects that may be deadly. Cipro and other fluoroquinolones weakening of collagen may lead to bulge or rupture in MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BAIR HUGGER COMPLICATIONS Injuries and Complications Associated with Bair Hugger. Serious complications developed after surgery using the Bair Hugger forced-air warming blanket device have included: Deep joint infections of hip and knee. Antibiotic resistant infections. Sepsis. Need for revision surgery to remove and replace device. ACTEMRA - LIVER FAILURE RISKS - CONSUMER SAFETY GUIDE Actemra, a medication used for the treatment of RA, has been linked to life-threatening side effects including liver failure, cardiovascular events and GI perforation. Genentech, manufacturer of Actemra, may be facing hundreds of lawsuits due to serious complications caused by the medication. People who have suffered liver failure, heart attack PENUMBRA JET 7 XTRA FLEX CATHETER RECALL Penumbra’s Recall of the JET 7 Reperfusion Catheter Due to Distal Tip Damage, U.S. Food and Drug Administration (01/29/2021); Penumbra’s Urgent Voluntary Recall of JET 7 Catheters with Xtra Flex Technology Due to Increased Risk of Mortality and Serious Injury – Urgent Letter to Health Care Providers, U.S. Food and Drug Administration (12/15/2020)POWER MORCELLATORS
Johnson & Johnson under FBI Investigation. Ethicon and Johnson & Johnson suspended the sale of power morcellators shortly after the safety communication was issued. The company stated it had always warned surgeons that the spread of malignant tissue as possible, but because the device was approved via the FDA’s fast track 510 (k)process and
TAXOTERE - SIDE EFFECTS AND WARNINGS - CONSUMER SAFETY GUIDE Taxotere Uses. Taxotere (docetaxel) is an antineoplastic agent used as chemotherapy to treat a number of types of cancer. It is used in combination with other drugs such as cisplatin, fluorouracil, doxorubicin, cyclophosphamide and prednisone and is approved to treat: VALSPAR EXTERIOR PAINT PROBLEMS Consumers who painted their homes with Valspar Exterior Paint noticed a number of problems shortly after the paint job was finished. Issues included: Bubbling. Peeling. Expansion. Buckling and warping of the vinyl siding. Valspar has not yet recalled its exterior paint product, but it might still be possible for homeowners to receive CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a SCAFFOLDING ACCIDENTS Scaffolding must include toeboards to eliminate the chance for accidentally kicking loose object over the edge. Scaffolds must be at least 10 feet from electric power lines. Scaffolds must be constructed and inspected by trained “competent” personnel. All employees who AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ABILIFY SIDE EFFECT WARNING Bristol-Myers Squibb (BMS), manufacturer of Abilify, has been the subject of thousands of lawsuits. These lawsuits have been filed by Abilify users who claimed that the manufacturer failed to adequately warn them of serious side effects including: Gambling and compulsive behaviors. Stroke. Hyperglycemia and Type 2 diabetes. BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. BONE CEMENT COMPLICATIONS Bone cement used to secure artificial joint devices during knee, hip or other joint replacement or stabilization surgery may loosen, fragment or cause serious life-threatening complications like bone cement implantation syndrome (BCIS). SURGE PROTECTOR FIRES Don’t modify grounded plugs by clipping of third prong. Avoid daisy-chain use of electric cords which are plugged into one another. Don’t overload circuits by plugging too many devices in at once. Replace worn parts or cords which have become damaged or frayed. If a SCAFFOLDING ACCIDENTS Scaffolding must include toeboards to eliminate the chance for accidentally kicking loose object over the edge. Scaffolds must be at least 10 feet from electric power lines. Scaffolds must be constructed and inspected by trained “competent” personnel. All employees who AESCULAP KNEE REPLACEMENT Aesculap knee replacements are causing recipients to experience painful side effects and require risky revision surgery. Doctors have discovered the bonding cement used to adhere the device in place is not working, leading to device loosening, pain, and loss of mobility. MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BENICAR SIDE EFFECTS Some side effects of Benicar may be more severe and may indicate a serious medical issue including low blood pressure, kidney disease, muscle breakdown (rhabdomyolysis) or high potassium levels (hyperkalemia). Taking other medications may increase the chance for severe side effects. Patients should tell their doctor or pharmacistabout all of
ABILIFY SIDE EFFECT WARNING Bristol-Myers Squibb (BMS), manufacturer of Abilify, has been the subject of thousands of lawsuits. These lawsuits have been filed by Abilify users who claimed that the manufacturer failed to adequately warn them of serious side effects including: Gambling and compulsive behaviors. Stroke. Hyperglycemia and Type 2 diabetes. BARD HERNIA MESH LAWSUIT Bard hernia mesh may have caused serious injuries in patients who received the implant during a hernia repair procedure. The Food and Drug Administration (FDA) has estimated that up to 90% of the near-one million hernia repair surgeries may use surgical mesh to stabilize abdominal or groin tissue. C.R. Bard, through its Bard Davol division,is
WEYERHAEUSER TJI JOISTS PROBLEMS Weyerhaeuser is facing legal action filed by homeowners affected by the defective products. These homeowners have a wide variety of allegations against the company, including breach of contract, consumer fraud, and negligence. They are concerned the use of the TJI Joists in their home could cause them to develop serious illnesses andthey must
CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the public of consumer product safety information involving products, drugs, and devices that are currently on the market. As an online resource sponsored by Seeger Weiss LLP, Consumer Safety Guide strives to provide accurate, relevant consumer safety information all in one place. MEDTRONIC MINIMED INSULIN PUMP RECALL LAWSUIT Medtronic Insulin Pump Recall. The FDA issued a safety alert on November 21, 2019, regarding a Class I recall for Medtronic MiniMed Insulin Pump. A Class 1 recall is the highest urgency recall which indicates that the device poses a high risk of serious injury or death. The safety notification stated that Medtronic was recalling thedevices due
CIPRO - AORTIC ANEURYSM OR DISSECTION - CONSUMER SAFETY GUIDE Cipro Aortic Aneurysm or Aortic Dissection. Cipro may interfere with collagen structure which may cause cartilage to become brittle and tear. This is the mechanism by which tendon rupture occurs but may also cause serious cardiac effects that may be deadly. Cipro and other fluoroquinolones weakening of collagen may lead to bulge or rupture in MEDTRONIC INFUSION SETS Medtronic MiniMed Insulin Infusion Set Recall. In September 2017, the FDA announced Medtronic was issuing a voluntary Class 1 recall of its MiniMed Insulin Infusion Sets, warning users the device could over-deliver insulin shortly after the set is changed. The BAIR HUGGER COMPLICATIONS Injuries and Complications Associated with Bair Hugger. Serious complications developed after surgery using the Bair Hugger forced-air warming blanket device have included: Deep joint infections of hip and knee. Antibiotic resistant infections. Sepsis. Need for revision surgery to remove and replace device. ACTEMRA - LIVER FAILURE RISKS - CONSUMER SAFETY GUIDE Actemra, a medication used for the treatment of RA, has been linked to life-threatening side effects including liver failure, cardiovascular events and GI perforation. Genentech, manufacturer of Actemra, may be facing hundreds of lawsuits due to serious complications caused by the medication. People who have suffered liver failure, heart attack PENUMBRA JET 7 XTRA FLEX CATHETER RECALL Penumbra’s Recall of the JET 7 Reperfusion Catheter Due to Distal Tip Damage, U.S. Food and Drug Administration (01/29/2021); Penumbra’s Urgent Voluntary Recall of JET 7 Catheters with Xtra Flex Technology Due to Increased Risk of Mortality and Serious Injury – Urgent Letter to Health Care Providers, U.S. Food and Drug Administration (12/15/2020)POWER MORCELLATORS
Johnson & Johnson under FBI Investigation. Ethicon and Johnson & Johnson suspended the sale of power morcellators shortly after the safety communication was issued. The company stated it had always warned surgeons that the spread of malignant tissue as possible, but because the device was approved via the FDA’s fast track 510 (k)process and
TAXOTERE - SIDE EFFECTS AND WARNINGS - CONSUMER SAFETY GUIDE Taxotere Uses. Taxotere (docetaxel) is an antineoplastic agent used as chemotherapy to treat a number of types of cancer. It is used in combination with other drugs such as cisplatin, fluorouracil, doxorubicin, cyclophosphamide and prednisone and is approved to treat: VALSPAR EXTERIOR PAINT PROBLEMS Consumers who painted their homes with Valspar Exterior Paint noticed a number of problems shortly after the paint job was finished. Issues included: Bubbling. Peeling. Expansion. Buckling and warping of the vinyl siding. Valspar has not yet recalled its exterior paint product, but it might still be possible for homeowners to receive Javascript must be enabled for the correct page displaySkip to Content
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WELCOME TO CONSUMER SAFETY GUIDE Consumer Safety Guide is here to help inform the general public of the risks some products, devices, and drugs have on American consumers.Learn More
CONSUMER SAFETY CATEGORIES The American public relies on manufacturers and governmental agencies to ensure that products sold in the U.S. are safe when used as directed. We have information about some of the latest safety issues involving drugs, medical devices, food and other products.Active Lawsuits
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Products sold in the US every day can cause very serious harm to the public. From defective baby products to the cars we drive every day. DANGEROUS DRUGS & MEDICAL DEVICES Thousands of people are injured every year because of dangerous drugs and defective medical devices. Drugs and devices that were given to patients by their health care providers and used according to instructions still caused serious harm.Learn more
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LATEST CONSUMER SAFETY NEWS Recalls, safety alerts and government agency warnings are issued frequently but may be missed by consumers. Read up on the consumer safety news of the day.View All
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by CSG Team October 24, 2019 JOHNSON & JOHNSON BABY POWDER RECALL Johnson & Johnson recently recalled 33,000 bottles of its baby powder after the FDA determined one bottle contained asbestos. The recall comes after years of claiming its products are asbestos-free and safe for consumers to use without risk of exposure to dangerous carcinogens. This is the first time the company has removed babypowder from
by CSG Team October 22, 2019 VAPING RISK CONTINUES TO RISE Vaping, still considered a safer alternative to smoking cigarettes, has caused nearly 1300 lung illnesses since June 2019. Twenty-six of these cases have proven fatal. The Centers for Disease Control and Prevention just released the latest numbers associated with vaping incidents, which includes data from 49 states, as well as WashingtonDC and the US
by CSG Team October 4, 2019 CLASS ACTION LAUNCHED AGAINST CELL PHONE COMPANIES OVER RADIATION RISK A class-action lawsuit has been filed against cell phone manufacturers Samsung and Apple after it was determined that radiation emitted by smartphones exceed government-established safety standards. The test was commissioned by the Chicago Tribune and determined that radiation exposure was higher than the legal safety limit. It was also determined that radiation from Apple’s iPhone by CSG Team March 25, 2020 JIMMY JOHN’S FACING ACCUSATIONS OF SERVING TAINTED VEGETABLES The FDA has issued a warning letter to Jimmy John’s claiming the sandwich shop served produce implicated in five outbreaks of salmonella or E. coli in the last seven years. According to the FDA, Jimmy John’s engaged in a pattern of receiving and selling cucumbers, clover sprouts, and other fresh produce that was believedto
by CSG Team January 15, 2020 CONSUMER SAFETY ADVOCATES URGE WARNING FOR DOLLAR TREE DOLL Consumer safety advocates from the New York Department of State’s Division of Consumer Protection are demanding there be a public warning for a doll sold this holiday season at Dollar Tree stores. According to the agency, the Fashion Doll tested positive for phthalate levels more than 200 times what can be in products sold to by CSG Team October 24, 2019 JOHNSON & JOHNSON BABY POWDER RECALL Johnson & Johnson recently recalled 33,000 bottles of its baby powder after the FDA determined one bottle contained asbestos. The recall comes after years of claiming its products are asbestos-free and safe for consumers to use without risk of exposure to dangerous carcinogens. This is the first time the company has removed babypowder from
by CSG Team October 22, 2019 VAPING RISK CONTINUES TO RISE Vaping, still considered a safer alternative to smoking cigarettes, has caused nearly 1300 lung illnesses since June 2019. Twenty-six of these cases have proven fatal. The Centers for Disease Control and Prevention just released the latest numbers associated with vaping incidents, which includes data from 49 states, as well as WashingtonDC and the US
by CSG Team October 4, 2019 CLASS ACTION LAUNCHED AGAINST CELL PHONE COMPANIES OVER RADIATION RISK A class-action lawsuit has been filed against cell phone manufacturers Samsung and Apple after it was determined that radiation emitted by smartphones exceed government-established safety standards. The test was commissioned by the Chicago Tribune and determined that radiation exposure was higher than the legal safety limit. It was also determined that radiation from Apple’s iPhone by CSG Team March 25, 2020 JIMMY JOHN’S FACING ACCUSATIONS OF SERVING TAINTED VEGETABLES The FDA has issued a warning letter to Jimmy John’s claiming the sandwich shop served produce implicated in five outbreaks of salmonella or E. coli in the last seven years. According to the FDA, Jimmy John’s engaged in a pattern of receiving and selling cucumbers, clover sprouts, and other fresh produce that was believedto
by CSG Team January 15, 2020 CONSUMER SAFETY ADVOCATES URGE WARNING FOR DOLLAR TREE DOLL Consumer safety advocates from the New York Department of State’s Division of Consumer Protection are demanding there be a public warning for a doll sold this holiday season at Dollar Tree stores. According to the agency, the Fashion Doll tested positive for phthalate levels more than 200 times what can be in products sold to by CSG Team October 24, 2019 JOHNSON & JOHNSON BABY POWDER RECALL Johnson & Johnson recently recalled 33,000 bottles of its baby powder after the FDA determined one bottle contained asbestos. The recall comes after years of claiming its products are asbestos-free and safe for consumers to use without risk of exposure to dangerous carcinogens. This is the first time the company has removed babypowder from
by CSG Team October 22, 2019 VAPING RISK CONTINUES TO RISE Vaping, still considered a safer alternative to smoking cigarettes, has caused nearly 1300 lung illnesses since June 2019. Twenty-six of these cases have proven fatal. The Centers for Disease Control and Prevention just released the latest numbers associated with vaping incidents, which includes data from 49 states, as well as WashingtonDC and the US
by CSG Team October 4, 2019 CLASS ACTION LAUNCHED AGAINST CELL PHONE COMPANIES OVER RADIATION RISK A class-action lawsuit has been filed against cell phone manufacturers Samsung and Apple after it was determined that radiation emitted by smartphones exceed government-established safety standards. The test was commissioned by the Chicago Tribune and determined that radiation exposure was higher than the legal safety limit. It was also determined that radiation from Apple’s iPhoneNext
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