Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
DePuy Recall of ASR Hip Implant Announced for 93K Devices August 30, 2010 Staff Writers Add Your CommentsJohnson and Johnson subsidiary DePuy Orthopaedics has officially announced its recall of two DePuy ASR hip replacement systems due an unreasonably high failure rate, which may have caused thousands of patients to experience pain and require a revision surgery for a second hip replacement.ย The DePuy ASR hip recall was reported on this site earlier this month, after information was posted on the FDA website. However, the company officially issued a press release last Thursday announcing the recall of DePuy ASR Hip Resurfacing Systems and DePuy ASR XL Acetabular Systems, confirming that about 93,000 of the devices were sold for implant in hip patients.According to information released by DePuy, new 2010 data from the National Joint Registry (NJR) of England and Wales shows that the ASR Hip Resurfacing System has a revision rate of approximately 12% and the ASR XL Acetabular System has a revision rate for 13%. Although those rates are across all sizes of the devices, the company noted that devices with head sizes smaller than 50 mm in diameter, and those implanted in female patients, were most likely to fail.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDePuy has recommended that patients with an ASR hip device see their surgeons for an evaluation, even if the hip implant does not seem to be causing a problem.ย The DePuy ASR is a metal-on-metal hip replacement system developed in 2005. Health care professionals have increasingly been warning about problems with metal-on-metal hip implants, which can shed metal particles into the body. The particles can damage soft tissue, cause inflammatory reactions and lead to bone loss.DePuy has indicated that it intends to provide ASR hip settlements to cover reasonable and customary costs for monitoring and treatment, including revision surgeries, that are connected with the defective hip implant. However, product liability lawyers have recommended that individuals contact an attorney before accepting any compensation to make sure their rights are protected and that they receive all of the benefits and money they may be entitled to through a DePuy ASR hip recall lawsuit.In recent months, a number of lawsuits over faulty DePuy ASR Cup implants have been filed. It is expected that the number of cases will continue to grow as Depuy ASR recall lawyers continue to investigate and review potential cases for individuals who have experienced problems and complications after hip replacement surgery involving the device. Tags: DePuy, DePuy ASR, Hip Replacement, Johnson and Johnson, Metal Hip Replacement, Metal-on-Metal Hip Image Credit: |More Lawsuit Stories Amazon Nitrous Oxide Death Lawsuit Set for Trial in December 2027 August 28, 2026 TikTok Settlement Over Child Privacy Violations Results in $400M Payment August 28, 2026 Harbor Freight Transmission Jack Failure Lawsuit Filed Over Crushing Hand, Arm Injuries August 28, 2026 1 Comments Rohany September 29, 2010 I think this latest recall, of the ASR XL Acetabular System and the ASR Hip Resurfacing system, could hurt Johnson & Johnson the most. Thatโs because there is growing evidence that the company continued to sell the product despite the fact that they knew it had a much higher than average failure rate. According to DePuy, approximately 10,000 patients (or 1 in 8 who received a DePuy ASR replacement unit) could require the revision (second) surgery. Experts suspect that the device is defectively designed, although DePuy has thus far denied this. PhoneThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Amazon Nitrous Oxide Death Lawsuit Set for Trial in December 2027 (Posted: 2 days ago)A federal judge has scheduled a nitrous oxide wrongful death lawsuit trial against Amazon.com for December 2027.MORE ABOUT: NITROUS OXIDE LAWSUITWhippet Injuries, Deaths Lead to Bill Seeking to Ban Retail Sale of Nitrous Oxide Canisters (08/14/2026)Flavored Nitrous Oxide Lawsuit Alleges Amazon Canisters Caused Womanโs Death (05/27/2026)Social Media Influencers Promote Nitrous Oxide Use Without Warning About Inhalation Risks (05/18/2026) Olympus Colonoscopy Lawsuit Over C. 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