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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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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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Colorado Woman Sues American Medical Systems Over Transvaginal Mesh Injuries

Parker Waichman LLP, a national law firm, just filed a lawsuit on behalf of a Colorado woman allegedly injured by transvaginal mesh products manufactured by American Medical Systems, Inc. The suit was filed on May 21, 2012 in the U.S. District Court for the Northern District of California (Case No. ...

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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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Fracking Releasing Hazardous Chemicals into Local Waterways

Fracking Releasing Hazardous Chemicals into Local Waterways

Study shows two hazardous chemicals—ammonium & iodide—are being released & spilled into Pennsylvania and W.Virginia waterways from fracking operations in Marcellus shale.

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FDA Warning for Bone Graft Products in Patients Under 18

FDA Safety Warning for Bone Graft Products in Patients Under 18

FDA issued safety alerts to patients, parents & guardians, bone graft devices w/recombinant proteins or synthetic peptides not to be the first treatment for 18 & under.

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British Health Agency Strengthens Warnings about Valproate

British Health Agency Strengthens Warnings about Valproate Risk in Pregnancy

Statement issued urging healthcare professionals to give women information on birth defects when Depakote and other valproate medicines are used during pregnancy.

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Indiana Woman Alleges Serious Injuries From Transvaginal Mesh Products

Parker Waichman LLP, a national law firm, just filed a lawsuit on behalf of a woman who suffered injuries after receiving transvaginal mesh implants. The lawsuit suit alleges that the transvaginal mesh created an unreasonable risk and directly caused her injuries.

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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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Pradaxa Named in Most FDA Adverse Event Reports for Deaths, Hemorrhage, Kidney Failure and Stroke

The controversial blood thinner, Pradaxa, surpassed all other drugs monitored by the U.S. Food & Drug Administration (FDA) in adverse event reports made to the agency last year. According to the Institute for Safe Medicine Practices’ (ISMP) latest QuarterWatch report, Pradaxa also topped the list for reports of deaths, ...

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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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