Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments
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.
Food Recalls Should Include Specific Stores, Retailers In Some Cases: FDA September 27, 2018 Russell Maas Add Your CommentsFederal safety officials have released a new guidance regarding food recalls in the United States, highlighting the need for notices to include specific stores that may have received or sold contaminated foods, to better inform the public and prevent the spread of illnesses.ย The U.S. Food and Drug Administration (FDA) announced a new food recall retailer disclosure guidance this week, which calls for manufacturers to publicize specific geographic and store information involving retailers known to have potentially contaminated on their shelves.When food recalls are initiated, the FDA typically works with companies to publicize labeling information, product descriptions, lot numbers, as well as photographs and state distribution information to allow customer to take a more accurate approach in identifying and discarding potentially harmful or contaminated products.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 COMPENSATIONAlthough the agency does disclose certain stores information when recalls are initiated, it does not release specific store information, due to the confidentiality of supply chain information between the distributor and retailer. This can make identifying recalled products much more difficult for the consumer if there is not a label.“We recognize the importance of providing consumers with actionable information related to recalled food products,” FDA Commissioner Scott Gottlieb said in a press release. “Thatโs why today the FDA issued newย draft guidanceย that describes situations when disclosing retail information for products undergoing recalls is appropriate.”The draft guidance seeks to release lists of the specific retailers and locations the recalled products may have been purchased from to better inform customers. The FDA has noticed there are many cases in which publicizing specific retailer information could protect consumers when the food is not easily identified, such as produce or ingredients within mixed salad. Listing the specific retailers could also prevent customer confusion and help prevent the spread of illnesses.The draft guidance outlines certain situations when the FDA would intend to make public the retail locations. These scenarios include, but are not limited to, Class I recalls, where it has been deemed that consumption of the food has a reasonable probability of causing serious adverse health consequences or death to humans or animals.Under the new guidance, FDA officials would be authorized to list retailers known to have sold or currently be selling food products linked to a foodborne illness outbreak. One example listed where specific retailer information could have helped prevent the spread of illness was the multi-state pre-cut melon recall that occurred earlier this year sickening over 60 individuals with Salmonella in five states.In the guidance, officials explained that if specific retailers had been identified by the melon suppliers, it could have prevented many individuals from becoming ill and would have helped remove the recall products from store shelves much quicker.The FDA would also publicize retailers known to have sold recall food products in situations where the products are not easily identifiable from its retail packaging and if the food is likely to be available for consumption.The guidance encourages retailers and suppliers to work with the FDA to identify specific retailers to help improve recall processes.The FDA is accepting public comment on the draft guidance over the next 60 days. Comments can be submitted electronically atย https://www.regulations.gov. Written comments can be submitted toย Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Room 1061, Rockville, MD 20852. All comments should be submitted to docket number FDA-2018-D-1752. 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: Food Poisoning, Food Recall Image Credit: Photo Credit: <a href="http://www.shutterstock.com/gallery-1409053p1.html?cr=00&pl=edit-00">Niloo</a> / <a href="http://www.shutterstock.com/editorial?cr=00&pl=edit-00">Shutterstock.com</a>More Lawsuit Stories Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments July 13, 2026 New Study Adds to Evidence Depo-Provera Injections Cause Meningioma Brain Tumor Risks July 13, 2026 Antibiotic Reaction Lawsuit Claims Medical Malpractice Resulted in Woman’s Death July 13, 2026 0 Comments InstagramThis 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 Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: today)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026) First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard 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) Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: 4 days ago)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)
Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments July 13, 2026
Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: today)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)
First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard 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)
Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: 4 days ago)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)