Tag Archives: Medical Device Recall

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Federal DePuy ASR Hip Implant Trials Likely to Start This Year

It looks as though the first trials in the DePuy ASR hip implant multidistrict litigation could begin sometime later this year. According to a report from Bloomberg News, during a status conference held yesterday in Florida, attorneys for both plaintiffs and the defense told U.S. District Judge David Katz that ...

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Geodon the antipsychotic drug can Cause Deadly Skin Reaction

Geodon can Cause Deadly Skin Reaction, FDA Warns

The FDA has required a new warning label for the antipsychotic drug Geodon (ziprasidone) to include the risk of a potentially fatal skin reaction.

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Exposure to Common Pesticide May Increase ADHD Risk

Exposure to Common Pesticide May Increase ADHD Risk

A new study has found that exposure to a common household pesticide may increase the risk of attention deficit hyperactivity disorder (ADHD) in children.

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Conspiracy Claims in Talcum Powder Case Survive Motion to Dismiss

Conspiracy Claims in Talcum Powder Case Survive Motion to Dismiss

E. District of Missouri denied motion to dismiss conspiracy claims. Lawsuit alleges the defendants conspired to misrepresent true dangers with use of talcum powder.

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Cancer Groups Call for E-cigarettes Regulation/Research

Two-Leading-Cancer-Groups-Issue-Call-for-Regulation-of-E-cigarettes-and-Research-on-Health-Risks

The American Society of Clinical Oncology & the American Association for Cancer Research called for government regulation & research of e-cigarettes on health effects.

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Federal Judge Certifies Medtronic Infuse Shareholder Class Action Lawsuit

A shareholder lawsuit alleging Medtronic Inc. illegally promoted the off-label use of its Infuse bone growth product has been granted class action status by U.S. District Judge Paul Magnuson of Minnesota. According to a report from Law360.com, the Medtronic Infuse off-label promotion lawsuit was filed by several institutional investors on ...

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Whistleblower Wins Retaliation - Canaveral National Seashore

Whistleblower Wins Retaliation Lawsuit

A whistleblower who reported misconduct at Canaveral National Seashore has won a retaliation ruling against the U.S. Department of Interior, Florida Today reports.

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Scientist Calls for Federal Regulations for Fracking Pollution

Hydraulic fracturing (fracking) drilling should be governed by federal regulations because its pollution has no awareness of state boundaries.

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Older Patients Face Heart Attack Risk Following Surgery

Older Hip Implant, Knee Replacement Patients Face Heart Attack Risk Following Surgery

An emerging report reveals that older hip implant and knee replacement patients face increased heart attack risks following surgery. The risk for acute myocardial infarction (AMI) was seen in the first two weeks after these surgical procedures.

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FDA Metal-On-Metal Hip Replacement Investigation Is Flawed, Researchers Say

The U.S. Food & Drug Administration’s (FDA) metal-on-metal hip replacement investigation is flawed, according to researchers.

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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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