Covidien Surgical Stapler Lawsuit Blames Defective Design for Botched Hernia Repair and Gastric Sleeve Surgery
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Ethicon Endo-Surgery Circular Stapler Recall Issued Due to Complications October 29, 2012 Russell Maas Add Your Comments More than 157,000 Ethicon surgical staplers have been recalled, due to problems with incomplete firing strokes that may cause faulty staple formation, potentially resulting in painful and severe internal complications for the patient. An Ethicon surgical stapler recall was first announced in August, after reports surfaced where surgeons experienced problems that required them to abandon use of the device during surgery due to difficulty firing it. On October 26, the FDA indicated that the action was categorized as a Class I recall for the Ethicon Endo-Surgery circular staplers, due to the potential risk it may pose for consumers. A Class I recall designation means that continued use of the device is likely to cause severe injury or death. Learn More About Surgery Staples Lawsuits Problems with surgical staplers may result in devastating injuries from internal surgery staples. Lawyers review cases nationwide. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Surgery Staples Lawsuits Problems with surgical staplers may result in devastating injuries from internal surgery staples. Lawyers review cases nationwide. Learn More SEE IF YOU QUALIFY FOR COMPENSATION These devices are used in the surgical treatment of prolapse and hemorrhoids, where circular or semicircular stapling of anorectal tissue is needed. Failure to complete the firing stroke of the stapler can result in severe pain, sphincter dysfunction, rectal wall damage, sepsis, bleeding, and occlusion of the rectal canal. Failure to complete the firing stroke can also result in poor staple formation, dehiscence of the rectal wall staple line and bleeding. The recall affects the following products: Ethicon PROXIMATE HCS Hemorrhoidal Circular Stapler and Accessories 33mm (Product Code: PPH01) Ethicon PROXIMATE PPH Hemorrhoidal Circular Stapler and Accessories 33mm (Product Code: PPH03) Ethicon TRANSTAR Circular Stapler Procedure Set (Product Code: STR10) The recalled surgical staplers were manufactured by Ethicon, a subsidiary of Johnson and Johnson, between April 16, 2011 and July 24, 2012 and distributed from April 18, 2011 to July 23, 2012. The initial Ethicon Endo-Surgery stapler recall was announced in August following complaints that the surgical staple guns were too hard to fire. In one case, a surgeon gave up trying to use the stapler mid-surgery due to frustration and an inability of the device to function properly. Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell 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 nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Ethicon, Johnson & Johnson, Surgical Error, Surgical Stapler More Surgical Staplers Lawsuit Stories Ethicon Surgical Stapler Recall Issued After Patient Died When Device Failed Mid-Surgery July 28, 2025 Covidien Stapler Malfunctioned During Surgery, Leading to Tissue Damage and Hospitalization: Lawsuit September 13, 2022 Covidien Surgical Stapler Lawsuit Blames Defective Design for Botched Hernia Repair and Gastric Sleeve Surgery June 9, 2022 3 Comments Daniel December 6, 2021 Case law suggests manufactures knew for 10 years prior to the recall. Any cases that happened within this time frame should be allowed. I need someone for a 2008 surgery. Natasha July 22, 2014 I have heard of multiple cases where this product has either killed or severely injured someone. There is so much negative information in the FDA’s MAUDE site about this product, please be careful. This is a dangerous product. Brandon October 30, 2012 I suffered necrotizing fasciitis, sever SEPSIS and underwent 19 additional surgeries (including a colostomy) after a staple broke open following a Hemorrhoidectomy in July 2012. A defective proximate pph circular stapler appears to be the culprit. 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 TermPhoneThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Dupixent Cutaneous T-Cell Lymphoma Warning Label Update Being Evaluated by FDA (Posted: yesterday) Federal regulators are investigating whether Dupixent increases the risk of cutaneous T-cell lymphoma (CTCL), after more than 300 adverse event reports flagged cancer diagnoses among users. The FDA’s review comes as lawsuits are being pursued nationwide, alleging Sanofi and Regeneron failed to warn that the blockbuster eczema drug could either trigger or mask the rare blood cancer. 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Ethicon Surgical Stapler Recall Issued After Patient Died When Device Failed Mid-Surgery July 28, 2025
Covidien Stapler Malfunctioned During Surgery, Leading to Tissue Damage and Hospitalization: Lawsuit September 13, 2022
Covidien Surgical Stapler Lawsuit Blames Defective Design for Botched Hernia Repair and Gastric Sleeve Surgery June 9, 2022
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