Tag Archives: Defective Medical Device Lawyer

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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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Post -Tonsillectomy Morphine Life-Threatening in Children

Post -Tonsillectomy Morphine can be Life-Threatening in Children, Study Finds

A new study published in Pediatrics suggests that morphine can result in life-threatening respiratory problems when given to children after a tonsillectomy.

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EMA Seeks Stronger Pradaxa Guidance for Bleeding Side Effects

Regulators in Europe have again asked Boehringer Ingelheim, the manufacturer of the blood thinner Pradaxa, to update the drug’s label with additional information regarding Pradaxa bleeding side effects. According to the European Medicines Agency (EMA), the new guidance should include more specific information on when Pradaxa must not be used, ...

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Cancer Groups Issue Statement for Regulation of E-cigarettes

Cancer Groups Issue Statement Calling for Research and Regulation of E-cigarettes

The American Society of Clinical Oncology & the American Association for Cancer Research are calling on the government to regulate e-cigarettes.

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Medtronic Infuse Studies Faulted for Downplaying Side Effects

Medtronic Inc.’s published studies for its Infuse bone graft product may have downplayed serious side effects, according to an analysis published last year in The Spine Journal. The study, which drew on U.S. Food & Drug Administration (FDA) documents and other data sources, suggests that up to half of ...

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U.K. Regulators Issue Additional Guidance for Metal-on-Metal Hip Implant Recipients

Regulators in the U.K. are once again issuing advice to doctors and other healthcare professionals involved in the follow-up of patients with metal-on-metal hip replacement devices. In an alert issued by the Medicines and Healthcare products Regulatory Agency (MHRA), guidance is provided for four groups of metal-on-metal hip implant ...

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Medtronic Settles Charges Over Kickbacks To Doctors

Medical device giant, Medtronic Inc., is settling charges over kickbacks to doctors. The firms just agreed to pay $23.5 million to settle claims it paid physicians kickbacks in exchange for their use of its pacemakers and defibrillators, according to a U.S. Justice Department announcement yesterday. The company was accused of seeking ...

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Medtronic Infuse Lawsuit Alleges Off-Label Use Cause Painful Complications

A man in Louisiana has filed suit against Medtronic Inc. over injuries allegedly cause by off-label use of its Infuse Bone Graft product. The plaintiff, who received Infuse during transforaminal spinal lumbar fusion surgery, claims that the bone growth protein caused unwanted bone growth along his spine, worsening the back ...

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Research Study Confirms Fracking Cause of Ohio Earthquakes

Research Study Confirms Fracking as Cause of Ohio Earthquakes

Fracking operation near Poland Township, Ohio, activated a previously unknown fault in the, causing 77 earthquakes with magnitudes ranging from 1.0 to 3.0 in March 2014.

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Tentative Ohio Fracking Regulations Criticized as too Lax

Lawmakers in Ohio have tentatively passed new regulations governing hydraulic fracturing (fracking) drilling but they’ve immediately been criticized for being too favorable to the natural gas and oil industries.

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Mirena® putting women at risk of suffering serious side effects

Women who opt for Mirena® as a contraceptive method are putting themselves at risk of very serious and sometimes life-threatening side effects. Mirena® is an intrauterine contraceptive that’s implanted in women and is designed to stay in the uterus for … Continue reading

Posted in Defective Medical Devices, Mirena IUD | Tagged , , |

Zimmer receiver FDA warning over manufacturing, testing processes at Puerto Rico facility

Medical device maker Zimmer Holdings Inc. has received a federal regulatory warning over invalid manufacturing and testing procedures being conducted on one of its hip implants. The company is currently engaged in ongoing legal battles over its allegedly defective line … Continue reading

Posted in Defective Medical Devices, NexGen LPS femoral component, Zimmer NexGen CR-Flex knee implants, Zimmer NexGen LPS femoral component, Zimmer NexGen MIS Tibial Components | Tagged |

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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Smith & Nephew Recalls IV PREP Antiseptic Wipes for Possible Bacterial Contaminati

Smith & Nephew’s Advanced Wound Management division just announced a U.S. voluntary nationwide recall of selected lots of its < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">IV PREP Antiseptic Wipes (product number 59421200) that were manufactured by The Triad Group. This recall follows a prior nationwide … Continue reading

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CT Scan Radiation Overdoses Reported at Cabell Huntington Hospital in West Virginia

Another large hospital is at the center of a scandal involving < "http://www.yourlawyer.com/topics/overview/Radiation-Overexposure-Medical-Devices-Lawsuit-Lawyer">radiation overdoses from CT scans. According to The New York Times, the CT scan radiation overdoses occurred at Cabell Huntington Hospital in Huntington, West Virginia for more than … Continue reading

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Cook Inc. Recalls Central Venous Catheter Trays for Leak Issue

Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays and Single and Double Lumen PICC Peripheral Inserted Central Venous Catheter Trays are being recalled, the U.S. Food and Drug Administration (FDA) just announced. Cook, Inc., located at 750 Daniels Way … Continue reading

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DePuy ASR Hip Implant Lawsuit Filed by Seven Forced to Undergo Revision Surgery

A < "http://www.yourlawyer.com/topics/overview/DePuy-Hip-Replacement-Implant-Recall">DePuy ASR hip implant lawsuit was recently filed by seven Rochester, New York residents who say they were forced to undergo revision surgery after their ASR hip failed prematurely. The DePuy ASR hip implant was recalled in August, … Continue reading

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