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.
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
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.
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.
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.
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.
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.
Walgreen’s Vitamin Recall Issued Over Lack of Child-Proof Caps June 12, 2015 Russell Maas Add Your CommentsWalgreenโs is recalling thousands of women’s multivitamin bottles, after recognizing the bottle cap design does not meet child-resistant standards, posing a potential health risk for young children if multiple tablets are ingested at once.ย The Walgreenโs Multivitamin Women 50+ tablets recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on June 11, after the manufacturer learned the bottle caps are not child-resistant and senior friendly as required by the Poison Prevention Packaging Act.The CPSC is urging consumers to place the vitamin bottles out of the reach of children immediately, due to the supplements containing iron, which can cause serious injury or death to young children if multiple tablets are ingested at once.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 COMPENSATIONThe recall involves “Well at Walgreens” brand name Multivitamin Women 50+ tablets containing UPC number 3-11917-17262-0 and lot numbers 000001 with expiration date September 2016, 000002 with expiration date December 2016, or 000003 with expiration date November 2016. The multivitamins were sold in white plastic bottles containing 200 tablets and has the wording โWell at Walgreens Multivitamin Women 50+โ printed on the bottleโs white and silver label. A yellow label at the top of the bottle states โValue Sizeโ.The CPSC requested the recall due to the potential dangers the pill bottles pose to young children and the designs failure to be senior-friendly. The Poison Prevention Packaging Act set forth by the American Association of Poison Control Center mandates that pills bottles must be designed or constructed to be significantly difficult for children under five years of age to open within a reasonable time, and not difficult for normal adults, the elderly, or handicapped to use.The multivitamins were manufactured in the U.S. under International Vitamin Corporation of Freehold, New Jersey where they were sold exclusively at Walgreens drug stores nationwide from January 2015 through March 2015 for about $16.Customers are being asked to immediately place the multivitamin bottles out of the reach of children and contact Vitamin Corp. at 866-927-5470 or visit them at www.ivcinc.com and navigate to the Safety Recall link for information on how to obtain a free replacement child-resistant cap.Walgreenโs has also announced a recall of Nice! Powdered Sugar Mini Donuts recall this week, due to a risk of mold on products sold exclusively at Walgreenโs stores.The powdered donuts were sold nationwide in 11.5 ounce packages and can be identified by the WIC number 178206 and UPC number 4902264948. Both product identification numbers can be located on the product bar code.Walgreenโs is asking customers to return the product to any Walgreens store for a full refund or contact the companyโs customer service at 1-800-925-4733 for further questions. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Children, Mold, Multivitamin, WalgreensMore Lawsuit Stories Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks August 18, 2026 IVF Lawsuit Alleges Defective PGT-A Testing Machine Led to Loss of Embryo August 18, 2026 Medtronic Seeks to Dismiss HeartWare HVAD Lawsuit Over Heart Pump Malfunction August 18, 2026 0 Comments X/TwitterThis 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 Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: today)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026) Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (Posted: yesterday)A federal judge has called for a meeting between attorneys representing plaintiffs and defendants in Covidien mesh lawsuits following an $88 million verdict against the manufacturers.MORE ABOUT: HERNIA MESH LAWSUITCovidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026) Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: 5 days ago)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026)
Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks August 18, 2026
Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: today)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)
Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (Posted: yesterday)A federal judge has called for a meeting between attorneys representing plaintiffs and defendants in Covidien mesh lawsuits following an $88 million verdict against the manufacturers.MORE ABOUT: HERNIA MESH LAWSUITCovidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)
Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: 5 days ago)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026)