If you had internal staples put in during surgery which later needed corrective surgery to fix, you may be affected by the recalled products and may meet the Ethicon lawsuit criteria. This risk has been cited as a reason behind surgical stapler recalls in recent years. Food and Drug Administration initiated a Class 1 recall—its most serious type of recall—of surgical staplers.
The largest surgical stapler lawsuit verdict was $80 million for a woman who suffered injuries during an operation that nearly killed her. As of 2019, the number of surgical stapler lawsuits is expected to climb. In fact, they are the manufacturers of the first sutures ever made.
Surgical Stapler Lawsuit FAQs
In recent years, they have also introduced several types of surgical staplers, such as Proximate, Echelon Flex, and many others. The company owns 80% of the US market for medical sutures and sells its products in 52 countries worldwide. These large range of numbers, however, only represent what the FDA has admitted in public. Kaiser Health News also reported that a whopping 56,000 reports of surgical stapler malfunctions included in the hidden database were never disclosed to the public. Victims of malfunctions and errors involving surgical staplers are already filing lawsuits.
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These staplers were distributed from March 15, 2018, and March 8, 2019. Johnson & Johnson initiated its recall of the staplers on April 11, 2019. If you suspect that you or a loved one may have been affected by the Ethicon stapler recall, please fill out ethicon lawsuit staples the form below or contact our office to schedule a free consultation. Our dedicated team of injury lawyers can listen to the facts of your case and explain your legal options for seeking justice and the full compensation that you rightfully deserve.
The Carolina Justice Report is a podcast from The Lovely Law Firm, located in Myrtle Beach, SC. The podcast features information, interviews and commentary on personal injury law, criminal law and community safety topics. The Lovely Law Firm represents clients in Myrtle Beach and surrounding areas with criminal and personal injury cases. In May 2019, Ethicon recalled Proximate® Endo-Surgery Intraluminal Staplers because they can malfunction and cause serious injury or death. It is not a substitute for professional medical advice, diagnosis or treatment. Any unauthorized or illegal use, copying or dissemination will be prosecuted.
The verdict was against Covidien, the surgeon, and the Southern Illinois University School of Medicine. Surgical staples are placed with a specialized instrument called a stapler. Staplers are manufactured by several companies, most notably, Ethicon (a branch of Johnson & Johnson, 3M, Covidien , and Stryker, among others.
The former acknowledged they had an exemption that allowed them to report adverse events to the FDA privately. There have been four other recalls since then as more injuries have surfaced. If you are expecting to undergo surgery, talk to your doctor about whether they will use staples.