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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Blair Chenille Robe Fires Lead to Expanded Recall for Jackets and Tops October 23, 2009 AboutLawsuits Add Your CommentsA chenille robe recall issued earlier this year has been expanded to include 138,000 women’s chenille tops, jackets and full-length robes, due to continuing reports of the garments catching on fire and causing at least nine deaths.The U.S. Consumer Product Safety Commission issued a release on Thursday notifying consumers that previous recalls issued by Blair LLC in April and June 2009 have been expanded after reports of four additional deaths that occurred when their chenille robes caught fire and at least one report involving another type of garmet made with the same material.Most of the chenille robe fires have occurred while the victim was cooking or near a flame, usually involving elderly women. The CPSC has said that the products fail to meet federal flammability standards.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 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 COMPENSATIONThe initial recall was issued on April 24, 2009 for 162,000 chenille robes after reports of severe burns and fires. Following additional reports problems with the robes, including several deaths, the robe recall was re-announced on June 11, 2009.The expanded chenille recall issued October 22, 2009, which now includes all women’s chenille clothing sold by the company, including women’s chenille jackets, women’s chenille lounge jackets, and women’s chenille tops. All of the items are made of plush sculpted chenille, with a label that says “100% Cotton, RN81700, Made in Pakistan.”The jackets are described as one-piece garments of plush sculpted chenille with three front buttons, pointed lapels, long sleeves and two front patch pockets. They come in gold, red, navy and hunter green, and were sold as item numbers 1392801, 1392802, 1392803, and 1392804.The lounge jackets are described as one-piece garments of plush sculpted chenille with a shaped stand collar, horizontal chenille front and back yolks and cuffs, and a full-button front with five matching button closures. The lounge jacket has long sleeves with self cuffs, a straight bottom with self hem, and two side seam pockets. The lounge jacket comes in lavender, aqua and light pink and were sold as item numbers 4526401, 4526402 and 4526403.The women’s chenille tops are also one-piece garments of plush sculpted chenille, and are pullovers with a rounded neckline, long sleeves, a straight bottom with side vents, and ribbed binding at the neckline and cuffs. The tops were sold in light purple, rose, dusty blue and sage green and were sold as item numbers 1811201, 18111202, 1811203, and 1811204.All of the recalled items were manufactured in Pakistan by A-One Textile & Towel. The recalled clothing was sold in Blair Catalogs and from the company’s website and Blair stores in Warren and Grove City, Pennsylvania, and Wilmington, Delaware, from July 2000 through April 2007.The CPSC urges consumers who have the garments to stop wearing them immediately and contact Blair LLC for information on how to receive a full refund or a $50 gift card. Tags: Chenille Recall, Product Liability, Robe Recall Image Credit: |More Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 2 Comments Ana November 14, 2009 They called my home phone today about this, even though I have never ordered anything chenille. They said they were contacting all of their customers. Sarah October 23, 2009 I have a full length robe from Blair that says 100% Cotton RN81700. It is lavender chenille. I do not have their address to notify them so that I can get a refund. I no longer have the catalog that I ordered it out of. The other number on it is by the size REG 1237711 I will stop wearing it but would like a refund as soon as possible so that I can replace it. FacebookThis 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a man’s chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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