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.
IKEA Crib Matress Recall Expanded Over Entrapment Risks May 4, 2015 Russell Maas Add Your CommentsIKEA has expanded a 2014 infant crib mattress recall, to include more than 300,000 units, after a government investigation determined that a greater range of designs may be unreasonably dangerous and defective, potentially allowing infants to become entrapped between the mattress and crib walls.ย The IKEA crib mattress recall expansion was announced by the U.S. Consumer Product Safety Commission (CPSC) on May 1, after an entrapment risk was identified among models not included in the original recall.At least two separate reports have been received involving infants who became trapped in the gap between an Ikea mattress and crib wall.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 original IKEA recall was first announced in January 2014, impacting nearly 170,000 mattresses that the CPSC deemed unsafe due to failure to meet size specifications. According to federal standards, a mattress is deemed to have a defective design if a gap between the mattress and crib ends are larger than two fingers width.The recall now includes roughly 344,000 IKEA SULTAN and VYSSA crib mattresses sold under the model names SULTAN BLUNDA, SULTAN DRรMMA, SULTAN SNARKA, SULTAN SUSSA, VYSSA VACKERT, VYSSA VINKA, VYSSA SPELEVINK, VYSSA SLรA and VYSSA SLUMMER. The recalled mattresses measure 52 inches long and 27 ยฝ inches wide and are marked with a manufactured date on or before May 4, 2014. Owners can identify the mattresses by the identification label. The label will have the date of manufacture in either Month-DD-YY or YY-WW format.The CPSC, the International Sleep Production Association (ISPA), and the American Society for Testing Materials (ASTM) worked jointly in 2013 to create a more stringent standard for crib mattress size requirements. The agencies now require manufacturers to include safety labels to warn customers to make sure their crib mattress properly fits within the crib to prevent children from becoming trapped in open space along the edges.The recalled mattresses were manufactured in Mexico, China, Poland, and the U.S. under IKEA North America Services LLC., of Conshohocken, Pennsylvania were they were sold exclusively at IKEA stores nationwide and online at www.ikea-usa.com from October 2000 to May 2014, for between $20 and $100.The CPSC recommends customers immediately stop using the recalled mattresses and inspect them by making sure there is not a gap larger than two fingers between the crib ends and the mattress. If there is such a gap, customers are being asked to return the mattress to any IKEA store for an exchange or a full refund. Customer may also contact IKEA customer service at (888) 966-4532 or view more about the recall by visiting www.ikea-usa.com and navigating to the โProduct Recallโ link. 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: Crib Matress, Ikea, SuffocationMore Lawsuit Stories Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial September 9, 2026 Lawsuit Alleges Apple AirTag Tracked Vehicle Location for Months September 9, 2026 Chlorpyrifos Autism Link May Involve Immune, Inflammatory Gene Changes: Study September 9, 2026 0 Comments CommentsThis 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 Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: today)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026) Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: yesterday)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026) Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 5 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: today)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: yesterday)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 5 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)