Tag Archives: Medical Device Recall

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New York Property Owners Challenge Binghamton Fracking Ban

According to a Reuters report, the landowners believe the Binghamton, N.Y., city council and Mayor acted against proper protocol when voting to ban fracking drilling the the city. Instead, they feel the city should have consulted with the Broome County Planning Commission before approving the ban.

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Pradaxa not Fit for a Dog, Family of Alleged Pradaxa Bleeding Victim Claims

The family of a Texas woman who died just months before her 60th wedding anniversary believes she would be alive today were it not for Pradaxa (dabigatran). According to a report from the Houston Press, Pradaxa patient Loraine Franklin fell and hit her head last December, resulting in an intracranial ...

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Study Suggests Hormonal Contraceptives Linked to Brain Tumor

Study Suggests Hormonal Contraceptives Linked to Increased Brain Tumor Risk

A study of Danish women of reproductive age suggests that long-term use of hormonal contraceptives is associated with an increased risk of brain tumors.

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DeflateGate’s Effects Impact Legal Gambling & the Economy

DeflateGate’s-Effects-Impact-Legal-Gambling-and-the-Economy

The NFL has initiated a probe into the New England Patriots following allegations that the team intentionally used overly deflated footballs.

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Oklahoma Woman Latest to Head to Court Over Alleged DePuy ASR Hip Implant Injuries

Lawsuits filed by alleged victims of DePuy Orthopaedics’ recalled ASR hip replacement devices continue to pile up in the multidistrict litigation currently underway in U.S. District Court, Northern District of Ohio. Most recently, a woman from Pryor, Oklahoma, filed suit alleging complications caused by a DePuy ASR hip implant ...

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Fracking Should be Kept 600m From Aquifers, Study Says

New research on the safety of hydraulic fracturing (fracking) suggests new wells should not be dug within 600 meters of a water aquifer because underground fractures can extend about that far from a dug well. According to a report from UK’s The Guardian newspaper, researchers and geologists at Durham University have ...

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Actos, Avandia May Up Risk for Diabetic Macular Edema

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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Soda Consumption Causes Early Puberty & Girls’ Cancer Risk

Soda Consumption Causes Early Puberty and Increases Girls’ Cancer Risk

Drinking just one-and-a-half cans of sugar-sweetened soda a day can bring on early puberty in girls and increase their breast cancer risk.

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FDA Advisory Panel Wrestling with Metal-on-Metal Hip Replacement Safety

An advisory panel for the U.S. Food & Drug Administration (FDA) began a highly-anticipated meeting yesterday to discuss the safety of metal-on-metal hip implants. Among other things, the panel of outside experts is being asked to make recommendations regarding the best practices for monitoring patients with metal-on-metal hip replacements. ...

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Dozens Receive Nonsterile Simulated Saline Solution

Dozens-Receive-Nonsterile-Simulated-Saline-Solution

The FDA said last week that more than 40 patients had received intravenous simulated saline that was not sterile and was not intended for human use.

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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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