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.
IKEA SNIGLAR Crib Recall Issued Due to Risk of Entrapment February 18, 2011 Staff Writers Add Your CommentsAbout 26,000 IKEA cribs are being recalled because some were sold with bolts that may be too short to secure the mattress support, which could cause them to collapse and pose a risk of serious injury or entrapment for an infant.ย The IKEA crib recall was announced on Thursday by the U.S. Consumer Product Safety Commission (CPSC) for the SNIGLAR cribs.Four bolts contained in the packaging for the crib are supposed to secure the mattress support. However, some of the cribs were shipped with bolts that are not long enough. If the mattress support detaches, then the crib could collapse, creating a risk of entrapment and suffocation for the child in the crib.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 IKEA crib recall affects 20,000 units sold in the United States and another 6,000 sold in Canada. The recall affects all SNIGLAR non-drop-side, full-size cribs. The cribs have SNIGLAR and model number 60091931 printed on a label attached to the mattress support. The cribs are made of natural and light-colored wood.The SNIGLAR cribs were sold at IKEA stores in the U.S. and Canada from October 2005 through June 2010 for about $80 and were made in Romania.The CPSC recommends that consumers immediately stop using the cribs and check them to see if the mattress support bolts extend through the nut. If they do, then they are the proper length and not affected by the recall. If they do not extend through the nut, the consumer should contact IKEA for a free repair kit and should find alternate sleeping arrangements for any child using the recalled crib.Consumers with questions can visit IKEAโs website at www.ikea-usa.com or call 1-888-966-4532.The recall came on the same day a study was published in the medical journal Pediatrics that found that almost 100,000 infants and toddlers are hurt in cribs and playpens every year. The injuries are usually the result of falls.ย The researchers looked at data on emergency room visits from 1990 to 2008 and found an average of about 26 infant and toddler injuries per day that could be linked to cribs, playpens, play yards, bassinets and similar infant and toddler furniture. There were at least 2,140 infant and toddler deaths as well, but researchers cautioned that the number could be higher because they did not factor in deaths of children who did not receive emergency room treatment. Tags: Children, Crib, Crib Recall, Cribs, Emergency Room, IkeaMore Lawsuit Stories Port Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection July 22, 2026 Sapien 3 TAVR Lawsuit Claims Valve Caused Iliac Artery Perforation, Wrongful Death July 22, 2026 Amazon Faces Lawsuit Claiming Defective Telescopic Ladder Caused Severe Injuries July 22, 2026 0 Comments LinkedInThis 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 Dupixent Caused Mycosis Fungoides Diagnosis (Posted: yesterday)A Dupixent cancer lawsuit claims the manufacturers failed to adequately test and label the eczema treatment, resulting in a CTCL cancer diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026)Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026) Fourth Uber Driver Sex Assault Lawsuit Bellwether Trial Set for Oct. 2026 (Posted: 2 days ago)A federal judge has scheduled the fourth bellwether trial involving claims that Uber failed to protect passengers from being sexually assaulted by its drivers for early October.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITUber Faces Investor Lawsuit Over Failure To Stop Driver Sexual Assaults (07/13/2026)Uber Sexual Assault Lawyers To Meet With MDL Judge Next Week, in Advance of Upcoming Trial (06/26/2026)Lyft Rideshare Assault Lawsuit Alleges Company Attempts To Silence Attack Victims (06/15/2026) Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (Posted: 5 days ago)Plaintiffs and defendants have submitted a joint schedule for a final pretrial conference before the second Bard PowerPort lawsuit bellwether trial over claims the port catheter is defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITNew Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)Jury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)
Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (Posted: yesterday)A Dupixent cancer lawsuit claims the manufacturers failed to adequately test and label the eczema treatment, resulting in a CTCL cancer diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026)Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)
Fourth Uber Driver Sex Assault Lawsuit Bellwether Trial Set for Oct. 2026 (Posted: 2 days ago)A federal judge has scheduled the fourth bellwether trial involving claims that Uber failed to protect passengers from being sexually assaulted by its drivers for early October.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITUber Faces Investor Lawsuit Over Failure To Stop Driver Sexual Assaults (07/13/2026)Uber Sexual Assault Lawyers To Meet With MDL Judge Next Week, in Advance of Upcoming Trial (06/26/2026)Lyft Rideshare Assault Lawsuit Alleges Company Attempts To Silence Attack Victims (06/15/2026)
Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (Posted: 5 days ago)Plaintiffs and defendants have submitted a joint schedule for a final pretrial conference before the second Bard PowerPort lawsuit bellwether trial over claims the port catheter is defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITNew Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)Jury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)