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.
Jardine Crib Recall Expanded: Total of 472,450 Cribs Now Recalled May 1, 2009 AboutLawsuits Add Your Comments The U.S. Consumer Product Safety Commission (CPSC) and Jardine Cribs have once again expanded a prior crib recall first issued last year, adding another 96,000 units to the list of potentially dangerous cribs. This is the third separate recall involving Jardine cribs sold exclusively at Babies “R” Us, Toys “R” Us, KidsWorlds and Geoffrey Stores, bringing the combined total number of cribs recalled to 472,450. This latest Jardine crib recall added seven models of wooden cribs with date codes between September 2005 and November 2007. Prior recalls were issued in June 2008 for 320,000 cribs, and in January 2009 for another 56,450 cribs. Potentially defective wooden slats on the sides of the crib could break, creating a gap large enough for an infant or toddle to become trapped. Do You Know about… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION At least 31 reports have been received of the wooden slats breaking, with 10 of the incidents involving children who broke the slats while they were in the cribs. Two of the confirmed reports involved children who became entrapped, but only minor injuries occurred. The recall list includes cribs with the following model and date codes, which were sold between September 2005 and April 2009 fro between $220 and $330: Drop-side Natural Olympia Single – Model # 0102B00 – Date Code Between 9/2005 and 1/2007 Drop-side Dark Pine Olympia Single – Model # 0102E00 – Date Code Between 9/2005 and 1/2008 Black Olympia Lifetime – Model # 0302P00 – Date Code Between 11/2005 and 5/2008 White Olympia Lifetime – Model # 0302C00 – Date Code Between 6/2006 and 12/2006 Americana Pecan 4-in-1 – Model # 0312D00 – Date Code Between 5/2006 and 11/2007 Antique Walnut Capri 4-in-1 – Model # 0308L00 – Date Code Between 12/2005 and 11/2007 Drop-side White Capri Single – Model # 0108C00 – Date Code Between 8/2006 and 11/2007 Consumers have been urged to immediately stop using the recalled Jardine cribs and to contact the manufacturer at (800) 646-4106 or visit www.jardinecribrecall.com. Many of the cribs recalled are drop-side cribs, which contain one side that lowers to make it easier for the parent to reach the child. Although this recall was not associated with problems with the drop side, Toys “R” Us announced last month that they are phasing the crib design out of their inventory following a number of major crib recalls and several infant deaths. Since the U.S. CPSC changed the way they analyze complaints in 2007 to identify patterns of products with particular products, a growing number of baby crib recalls have been issues as a result of defective designs which could pose an entrapment or strangulation hazard. Tags: Childrens Furniture, Childrens Furniture Recall, Crib, Crib Recall, Jardine, Jardine Crib Recall Image Credit: | More Lawsuit Stories High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims April 6, 2026 Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit April 6, 2026 Silica Dust Lawsuit Alleges Manufacturers Knew of Silicosis Risks From Quartz Countertops April 6, 2026 2 Comments Bernice August 11, 2014 We own the Jardine – Drop-side Black Olympia Single โ Model # 0102P00 โ Date Code 04/2006. So I am wondering how this bed could be any different/any safer than the EXACT same beds that have been recalled. The ONLY difference is the COLOR. This does not make sense, only certain Babies ‘R; Us stores carried the black color, so I think this may have been overlooked in error! Someone needs to check this information. PLEASE. I still have my original receipt! Drop-side Natural Olympia Single โ Model # 0102B00 โ Date Code Between 9/2005 and 1/2007 Drop-side Dark Pine Olympia Single โ Model # 0102E00 โ Date Code Between 9/2005 and 1/2008 Bernice August 11, 2014 Seriously, Jardine has recalled the EXACT same bed…EXACT same model with the only difference being that our bed is black in color # 0102P00 Drop-Side Olympia Single date 04/2006. They recalled the natural color # 0102B00 Drop-Side Olympia Single AND the dark pine color .# 0102E00 Drop-Side Olympia Single, both with the same dates as we have! So, can anyone please tell me how being a different color can make any difference at all. My opinion of this is that only a few Babies ‘R’ Us stores carried the bed in black and somehow this has been overlooked in the recall. URLThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: today) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026) Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 3 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026) Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 4 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)
Silica Dust Lawsuit Alleges Manufacturers Knew of Silicosis Risks From Quartz Countertops April 6, 2026
High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: today) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026)
Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 3 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 4 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)