Tag Archives: Recall

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Medtronic Sprint Fidelis Leads Vulnerable to Fracture after ICD Switch

Medtronic Sprint Fidelis leads are vulnerable to fracture following ICD switch, says a new study published in the June issue of the journal Heart Rhythm.

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Actos Bladder Cancer Lawsuit Filed by West Virginia Resident

Actos (pioglitazone) continues to be named in lawsuits alleging long-term use of the type 2 diabetes drug caused patients to develop bladder cancer. Just last week, the national law firm of Parker Waichman LLP filed suit against Takeda Pharmaceuticals on behalf of a West Virginia man who developed bladder cancer ...

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Transvaginal Mesh a Nightmare for Thousands of Women

Thousands of women who have received transvaginal mesh surgical implants to treat stress urinary incontinence (SUI) and pelvic organ prolapse (POP) are now living a nightmare, thanks to debilitating pain, bleeding, infection and other serious complications. According to the Sun-Sentinel, many of the women injured by transvaginal mesh claim ...

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Three Injured, Long Island Railroad Train Hits Car on Tracks

Three Injured When Long Island Railroad Train Hits Car on Tracks

3 people, injured on Wednesday at 1:20 p.m. when a LIRR train hit a livery cab on the tracks west of Wyandanch station. The train engineer, who suffered a shoulder injury.

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Actos Side Effects Lawyers Says Whistleblower Revelations Could Boost Bladder Cancer, Heart Failure Lawsuits

An attorney with a prominent personal injury law firm says an Actos whistleblower lawsuit filed earlier this year could strengthen legal claims alleging the type 2 diabetes medication caused some users to develop bladder cancer and heart failure.

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MTA Bus Crash and Two Cars Injures 23 at Utica Ave. & Clarendon Rd

Crash Involving MTA Bus and Two Cars Injures 23

Police are investigating an accident in Brooklyn on Wednesday afternoon that injured 23 people, 3 of them critically, when a car was knocked into the path of an MTA bus.

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Tennessee Resident Files Pradaxa Bleeding Lawsuit Following Cerebral Hemorrhage

A man from Tennessee has filed a lawsuit against the maker of Pradaxa, claiming that the blood thinner caused him to suffer a cerebral hemorrhage. The complaint alleges Boehringer Ingelheim Pharmaceuticals, Inc. concealed knowledge that Pradaxa can cause Serious, life-threatening bleeds, and did not warn that Pradaxa bleeding side effects ...

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Johnson & Johnson’s Ethicon Division to End Sales of Gynecare Prolift, Three Other Transvaginal Mesh Devices

Johnson & Johnson’s Ethicon Inc. division revealed yesterday that it will end sales of its Gynecare Prolift device and three other transvaginal mesh products. The plan to stop selling the four products was set forth in a letter filed by the company in the Ethicon transvaginal mesh multidistrict litigation ...

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Actos Whistleblower Lawsuit Questions Avandia Researcher's Financial Ties to Takeda

A prominent researcher has been implicated in an alleged cover-up of Actos side effects, according to a report from TheHeart.org. An Actos whistleblower lawsuit unsealed earlier this year has alleged financial connections between the Cleveland Clinic’s Dr Steven Nissen and the maker of Actos “should be considered when analyzing Actos’s ...

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Former Executives Accuse Health Technology Firm of Fraud

Former Executives Accuse Health Technology Firm of Fraud

Former NantHealth executives claim that the company made fraudulent claims about the reliability of its system, which links patient information gathered by the devices.

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Sweet Leaf Recalls Teas in Glass Bottles for Possible Glass Fragments

SweetLeaf

On December 10, the Sweet Leaf Tea Company announced a voluntary recall of Sweet Leaf Tea in 16-ounce glass bottles because of the possible presence of glass fragments. This was the result of glass breakage during the filling process. Consumers … Continue reading

Posted in Defective Products, Food Products, Product Recalls, Recalled Food Products | Tagged , , , , , |

Class 1 Recall for eVent Ventilators: Ventilator May Shut Off without Sounding Alarm

event_medical_inspiration

Medical device maker eVent Medical is recalling the LS, 5i, or 7i Inspiration ventilators because a faulty switch on the ventilators’ power board may fail, causing the ventilator to shut down without sounding an alarm. If the ventilator shuts down, … Continue reading

Posted in Defective Medical Devices, Health Concerns | Tagged , , , , |

FDA Orders Custom Ultrasonics to Recall AERs Used to Clean Duodenoscopes

FDA order Recall on AERs Used to Clean Duodenoscopes

The U.S. Food and Drug Administration (FDA) has ordered Custom Ultrasonics to recall all of its automated endoscope reprocessors (AERs), devices used to sterilized special medical scopes such as duodenoscopes. According to a Nov. 13 announcement, the recall is being … Continue reading

Posted in Defective Medical Devices, Duodenoscope, Legal News | Tagged , , , , |

Hamilton G5 Ventilators Recalled Due to Risk of Alarm Failure

Hamilton G5 Ventilators Recalled Due to Risk of Alarm Failure

Hamilton G5 ventilators, which are used to provide breathing support to adults, children, infant and newborn patients in health care facilities, have been recalled. According to a recall notice posted on the U.S. Food and Drug Administration’s (FDA)’s website, the … Continue reading

Posted in Legal News | Tagged , , , , |

General Motors Recalls Cars at Risk for Engine Fires, Some for the Second Time

General Motors Recalls Cars at Risk for Engine Fires

More than 1,300 General Motors cars have caught fire even after a recall repair that was supposed to prevent an engine fire. GM has acknowledged that the repair did not work. The company issued a new recall for 1.4 million … Continue reading

Posted in Defective Products, Motor Vehicles, Product Recalls, Recalled Vehicles | Tagged , , , , |

Sure Signal Heat-Activated Fire Alarms Recalled Due to Failure to Alert Consumers to a Fire

Sure Signal Heat-Activated Fire Alarms Recalled

Sure Signal Products has recalled more than 375,000 heat-activated fire alarms because a defective sensor can cause the alarm to fail to alert consumers of a fire. The Consumer Product Safety Commission (CPSC) has announced the recall on its web … Continue reading

Posted in Defective Products, Product Recalls | Tagged , , , , |

Texas Compounding Pharmacy Recalls Possibly Contaminated Sterile Drug Products

Texas Compounding Pharmacy Recalls Contaminated Products

A Dallas, Texas compounding pharmacy that has previously been cited for safety issues by the Food and Drug Administration (FDA), once again faces problems with the federal drug regulator. Downing Labs in Farmers Branch was cited for failing to investigate … Continue reading

Posted in Health Concerns, Pharmaceuticals | Tagged , , , |

Due to Fire Risk, Toyota Recalls 6.5M Cars

Due to Fire Risk, Toyota Recalls 6.5M Cars

Due to a defect in the driver’s side window that presents a fire hazard, Toyota is recalling 6.5 million vehicles. The recall affects roughly 2 million cars in the US. The problem is that the power-window master switch may have … Continue reading

Posted in Legal News, Product Recalls, Toyota Recall | Tagged , , , , |

GoGo squeez Recalls Applesauce

GoGo squeez Recalls Applesauce

Due to the presence of mold, snack brand GoGo squeeZ is voluntarily recalling pouches of applesauce. The affected products, which were made in the US, have a “best before date” between June 30, 2016 and July 26, 2016. The company … Continue reading

Posted in Legal News | Tagged , , , , |

Aspen Foods Frozen Chicken Recalled Due to Salmonella Risk

Aspen Foods Frozen Chicken Recalled Due to Salmonella Risk

Due to potential salmonella risks, Aspen Foods is recalling roughly 561,000 pounds of frozen, raw stuffed and breaded chicken products. The recall affects items produced between August 25 and September 17 and have ‘best if used by’ dates of August … Continue reading

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