Tag Archives: Medical Device Recall

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Exploding Tanks Kill Jeep Drivers 18 months after Recall

Exploding Gas Tanks Continue to Kill Jeep Drivers 18 months after Recall

Chrysler recalled Jeeps with exploding gas tanks more than 18 months ago, but 1 million+ of these vehicles have not been fixed as the death toll continues to rise.

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Majority of Metal-on-Metal Hip Implant Failures Occur within Two Years, Study Finds

A newly published metal-on-metal hip replacement study is reporting that the majority of failures occur early, within two years of surgery. The study, published in the journal Orthopedics, is just the latest to indicate that close follow-up of metal-on-metal hip implant patients is warranted.

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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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Metal-on-Metal Hip Replacement Concerns Grow in Canada

Canadian patients and doctors are voicing more concerns about metal-on-metal hip replacements, as health regulators around the world continue to investigate the safety of the devices. According to a report from the CBC, four companies have recently either recalled or suspended sales of metal-on-metal hip replacement devices, while a number ...

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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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Smokers More Vulnerable to Joint Replacement Failures

People who smoke cigarettes before and after receiving a total joint replacement, such as a hip replacement device or knee implant, are far more likely to endure revision surgeries on those implants than people who don’t smoke.

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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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Study Links Liquid in E-Cigarette to Viral Infections

Study Links Liquid in Electronic Cigarette to Increased Risk of Viral Infections

The National Jewish Health study, links the liquid used in e-cigarettes to a higher risk of respiratory viral infections, whether the liquid contains nicotine or not.

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FDA Urged to Ban Powdered Caffeine

FDA Urged to Ban Powdered Caffeine

Pennsylvania Senator Robert Casey has written to the Food and Drug Administration (FDA) to urge the agency to ban powdered caffeine, a dietary supplement.

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Neptune Waste Management System Recalled by Stryker Following Patient Death

Two serious injuries, including a death, have prompted a recall of the Stryker Neptune Waste Management System, a medical device that has never gained regulatory approval. According to a Bloomberg report this week, medical device giant Stryker Corp. has been … Continue reading

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Covidien Recalls Shiley Adult Tracheostomy Tubes

Covidien just announced a recall of its Shiley Adult Tracheostomy Tubes, the U.S. Food & Drug Administration said.  The Shiley Adult Tracheostomy Tube recall has been deemed Class I by the FDA, which means there is a reasonable probability that … Continue reading

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Class I Recall Issued for Smiths Medical Medfusion 4000 Syringe Infusion Pump

A Class I recall was just issued for Smiths Medical Medfusion 4000 Syringe Infusion Pump, the U.S. Food & Drug Administration (FDA) just announced. Class I recalls are the agency’s most serious recall designation and involve situations in which there … Continue reading

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B.Braun Recalls Infusomat Space Infusion System

B. Braun just issued a recall of its Infusomat Space Infusion System over the potential for breakage of an anti free flow flip catch, the U.S. Food & Drug Administration (FDA) just announced. The recall was designated a Class I … Continue reading

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CareFusion EnVe Ventilator Recall Deemed Class I

The CareFusion EnVe Ventilator recall has been deemed a Class I, the U.S. Food & Drug Administration (FDA) just announced. A Class I is the agency’s most serious designation and is defined as having a reasonable probability of serious adverse … Continue reading

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Waterpik to Replace SinuSense™ Water Pulsator Device Over Consumer Complaints

Waterpik, Inc., is replacing its SinuSense™ Water Pulsator device over consumer complaints, the U.S. Food & Drug Administration (FDA) just announced. Specific SinuSense™ Water Pulsator nasal irrigation devices Waterpik manufactured between May 2010 and July 2011 are involved in the … Continue reading

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DePuy ASR Hip Implant Lawsuit Filed by Connecticut Woman

The first Connecticut lawsuit against the maker of the recalled, defective < "http://www.yourlawyer.com/topics/overview/DePuy-Hip-Implant-Recall-Johnson-and-Johnson">DePuy ASR hip implant has been filed. Patricia Sorrentino-Galello underwent a second hip replacement just three years after her original surgery at Milford Hospital, the CT Post reports. … Continue reading

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Triad Group Shuts Down Line That Made Tainted Wipes

After several recalls, one nationwide; Bacillus cereus contamination; and links to a number of illnesses and one death, the Triad Group of Harland, Wisconsin is shutting down the line that manufactured < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">tainted alcohol prep products, pads, wipes, and swabs. … Continue reading

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Recalled DePuy Hip Implant May Be Failing at Much Higher Rate than First Thought

How likely are premature failures of th< "http://www.yourlawyer.com/topics/overview/DePuy-Hip-Implant-Recall-Johnson-and-Johnson">e DePuy ASR XL Acetabular Hip Replacement System? When DePuy Orthopedics issued recalls for the ASR XL Acetabular Hip Replacement System and the ASR Hip Resurfacing System last August, the company said data … Continue reading

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Johnson & Johnson’s Animas Unit Recalls Insulin Pump Cartridges

Following a year of unprecedented recalls, another unit of embattled drug giant, Johnson & Johnson, is issuing a medical device recall, this time, for < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">2.0 mL Animas Insulin Pump Cartridges. Some 2.0 mL insulin cartridges shipped between November 30, … Continue reading

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