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.
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.
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.
Shermag Drop-Side Crib Recall Issued After Reports of Hardware Failure September 30, 2011 Staff Writers Add Your CommentsAbout 3,100 Shermag drop-side cribs are being recalled after reports suggest the hardware may be prone to fail, posing a serious and potentially life-threatening risk for infants.ย The Shermag drop-side crib recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on September 29, after the commission and the manufacturer received at least 21 reports of incidents where the drop-sides detached from the crib or otherwise failed.While there have been no injuries reported in association with the recalled Shermag cribs, hardware problems with drop-side cribs made by a number of different companies have been associated with an alarming number of infant deaths and other injuries in recent years, leading the CPSC to recently ban the manufacture and sale of all drop-side crib designs.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 COMPENSATIONIf the drop-side rail hardware fails, the side can detach, leaving a gap in which an infant can become entrapped and potentially suffocate or strangle. A broken drop side could also allow a child to fall out of the crib unexpectedly and suffer injury.This latest recall affects about 2,300 Shermag drop-side cribs sold in the U.S. and about 800 sold in Canada separately or as part of the “City Lights,” “Fairy Tales” and “Dormez Vous” furniture collections. The recalled cribs have the model numbers 202647, 211047 and 272547, which is located on stickers and warning labels on the crib’s headboard or footboard. The cribs will have “Shermag” printed on a tag on the mattress springs as well.The cribs were sold at The Land of Nod and other baby specialty stores for between $400 and $800 from September 2004 through December 2008.A drop-side crib ban enacted by the CPSC went into effect in June 2011, after the commission voted in December to stop the sale, resale and manufacture of all cribs featuring the drop-side design. The vote came after at least 32 infant and toddler deaths were associated with drop-side cribs since 2000.The cribs are designed to allow easy access to the baby by having one side that can be unlocked and lowered. They have been particularly popular with shorter parents or those with back problems who have difficulty reaching over the rails of a standard crib.Consumers with the recalled Shermag drop-side cribs should stop using them immediately and contact Shermag to receive a free repair kit. In the meantime they should make alternative sleeping arrangements for any child using the affected drop-side cribs.Customers with questions can call Shermag at (800)567-3419 or visit the company’s website at www.shermag.com. Tags: Childrens Furniture Recall, Crib Recall, Cribs, Drop Side Crib, StrangulationMore Lawsuit Stories Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026 Indoor Fire Pit Lawsuit Indicates Flame Jet Set User’s Body on Fire August 20, 2026 Missouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit August 20, 2026 0 Comments 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 Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: today)A California woman’s Dupixent lymphoma lawsuit claims the manufacturers knew of the eczema drug’s cancer risks, but refused to inform doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (08/11/2026)CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026) FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: yesterday)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)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)
Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026
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