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.
Diabetes Glucose Test Strip Recall Issued Due to False Low Readings December 23, 2010 AboutLawsuits Add Your CommentsAbbott Laboratories has issued a recall for about 359 glucose test strips sold under a variety of brand names, such as Precision Xceed Pro, Precision Xtra, MediSense Optium, Optium, Optium EZ and ReliOn Ultima. The blood-sugar test strips may provide a false low reading, posing a potential health risk for diabetics.The diabetes glucose test strip recall was announced by the FDA and Abbott on Wednesday, warning diabetics who use the devices to test their blood sugar levels, that the test strips may provide false low readings.Test strips affected by the recall were manufactured between January 2010 and May 2010, and were used with the following blood glucose monitoring systems: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 COMPENSATIONPrecision XtraPrecision Xceed ProMediSense OptiumOptiumOptium EZReliOn UltimaProblems with the blood glucose test strips involve a defect that limits the amount of blood that is absorbed by each strip, which may lead to false results. According to the FDA, the risk of a false low reading is increased if the blood sugar test strips are exposed to warm weather or stored for long periods of time.Diabetes patients rely on the readings from the test strips to monitor their blood sugar levels. If a false low reading from the test strip is given, it may cause consumers to unnecessarily raise their blood glucose or to fail to treat elevated blood glucose.Abbott has offered to replace any of the recalled glucose test strips. To determine whether a test strip is affected by the recall, consumers can contact Abbott Diabetes Care at 1-800-448-5234 or visit www.precisionoptiuminfo.com to look up test strip lot numbers.Individuals who are impacted by the glucose test strip recall have been advised to use an alternate method to measure blood sugar levels or to purchase at least two weeks worth of new test strips while they wait for free replacements to be provided by Abbott.The FDA has also recommended that diabetes patients monitor the amount of time it takes to for their blood-glucose meter to start the “countdown” after blood is applied to the test strip. If the meter takes longer than five (5) seconds to start the countdown, the test strip is likely defective and the results should not be used. Also, if the reading from a strip is lower than would be expected or does not match the way a diabetes patient feels, the FDA has recommended that they contact their health care provider. Tags: Abbott, Diabetes, Diabetes Test Strip, Glucose Test StripMore 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 michael August 7, 2011 i used the relion strips and insulin for years, saw a report on local tv and havent seen an update since, i investigated the story and found that indeed i had packages of recalled strips, no contact from local walmart,, i went to walmart pharmicy and asked them about it they insted of trying to help me they just wanted to know how i knew of recall, ispoke with pham manager and was told there was noything they could do for me, since i had several boxes of recalled test strips i got upset and was asked not to return to their pharmacy chery January 11, 2011 I’m wondering why I was not told about these test strips. I use reli brand ,my name is in their computer. The way I found out was I went to get more and there were none on the shelf,even then no one knew why. I found out the next day when I went back. How ae they going to re-pay for the faulty ones? CompanyThis 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: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs 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: 3 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: 4 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)
Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs 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)
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