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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 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 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 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 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. 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
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 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
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
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 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 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 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. 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
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 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
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
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
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 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
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
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:ERB'S PALSY
Lack of movement in one hand. Lack of movement in lower arm on one side. Lack of movement in the entire arm on one side. Limpness in one arm. One arm held bent against the body. No feeling in arm or hand on one side. Weakness in one arm with a weakened grip. If symptoms of Erb’s palsy appear, the pediatrician should perform a physical exam PAM COOKING SPRAY FIRES Conagra issued a statement following the filing of the lawsuits claiming their cooking spray products are safe and explaining: “Please know the safety of our products and our consumers is always our top priority. When PAM is used correctly, as instructed, it is a 100-percent safe and effective product. All PAM Cooking Sprays includelarge
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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 May 15, 2020 POPULAR CRUISE SHIP LINE FACING LEGAL ACTION OVER COVID-19 DEATHS Legal claims have been filed against Princess Cruise Lines after passengers died of COVID-19 while onboard the company’s ships. According to the claims, the popular cruise line was negligent and mishandled notifying passengers that certain passengers and crew had been exposed to the virus. Legal experts say it could be difficult forpassengers to prove
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 May 15, 2020 POPULAR CRUISE SHIP LINE FACING LEGAL ACTION OVER COVID-19 DEATHS Legal claims have been filed against Princess Cruise Lines after passengers died of COVID-19 while onboard the company’s ships. According to the claims, the popular cruise line was negligent and mishandled notifying passengers that certain passengers and crew had been exposed to the virus. Legal experts say it could be difficult forpassengers to prove
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
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