11/17/2023 0 Comments Endo stapler ethicon![]() ![]() In general, surgical stapler lawsuits can compensate injured parties for: Douglas obtained a jury verdict of $8.5 million against Johnson & Johnson subsidiary, Ethicon Endosurgery, on behalf of the family of a 45-year-old man who died after a staple gun misfired during a weight-loss surgery.ĭouglas & London defective products senior attorney Virginia Anello also reached a significant confidential settlement on behalf of the family of a 31-year-old father of two who untimely passed away due to the malfunctioning of a staple gun during a lobectomy procedure. This isn’t the first time our firm has successfully faced Johnson & Johnson due to damages caused by a defective stapler. How Much Are Surgical Stapler Lawsuits Worth? New York State limits the amount of time you have to file a lawsuit, so do not delay in reaching out to Douglas and London to discuss your claim during a free case review. Sometimes the damage is not discovered until a follow-up visit, trip to the Emergency Room, or a later surgery. However, in other cases, complications from this defective device take longer to discover. In some instances, it is obvious to the surgeon that the stapler caused damage during surgery. Cases that qualify for a lawsuit include those where surgeries took place during those two months. These staplers were distributed for use in August and September of 2019. Who Might Qualify for an Ethicon Surgical Stapler Lawsuit?Ī total of 8,256 staplers were recalled by the FDA. Our team of investigators can get to the bottom of what happened to you or your loved one. Echelon Flex 60 Powered Plus Articulating Endoscopic Linear Cutter, 34cm Shaft Length (PSEE60A)Įchelon Flex Endopath Staplers Product Codes:Ĭontact a surgical stapler lawyer at Douglas & London if you are unsure what type of stapler was used during a recent procedure.Echelon Flex 60 Powered Plus Articulating Endoscopic Linear Cutter, 44cm Shaft Length (PLEE60A).Echelon Flex 60 Powered Plus Compact Articulating Endoscopic Linear Cutter (PCEE60A).Echelon Flex 60 Endopath Stapler, Articulating Endoscopic Linear Cutter (EC60A).Recalled Echelon Flex Endopath Staplers include: Malformed staples that are not recognized or addressed right away can lead to: Damage caused by the malformed staples required additional surgery to repair the faulty closures.īased on these serious defects in the Flex Endopath Staplers, the FDA issued a Class I recall, the most serious recall category reserved for devices that cause significant risk of bodily harm or death. The device was recalled due to a defect in a part that caused the staples to improperly close incisions, leading to leakage and bleeding at these sites. This surgical stapler, which is manufactured by Johnson & Johnson’s Ethicon division, was developed to cut and staple internal tissue together simultaneously during procedures. Johnson & Johnson has issued a recall of its Echelon Flex Endopath Staplers. COVID-19 Business Interruption Insurance FAQ.Xarelto Settlement & Disbursement Process FAQ.Allergan BIOCELL Breast Implant Recall Lawsuit.Hair Straightener & Hair Relaxers Uterine Cancer Lawsuits.3M Defective Combat Arms Earplug Lawsuit.Ethylene Oxide & Commercial Sterilizing Lawsuits.Camp Lejeune Water Contamination Lawsuit.Ethicon Echelon Flex Surgical Stapler Lawsuit Attorneys.Elmiron Lawsuit Lawyers in New York City.COVID-19 Business Interruption Insurance Denial Claims.The surgical staplers were manufactured between Maand March 6, 2019, and distributed between Maand March 8, 2019. The following product codes are involved in this Class 1 Recall: CDH21A, CDH25A, CDH29A, CDH33A, ECS21A, ECS25A, ECS29A and ECS33A. This recall involves a total of 92,496 Endo-Surgery Curved and Endo-Surgery Endoscopic Curved Intraluminal Staplers with adjustable height staples that are designed to permit a proper matching of the staples to the diameter of the lumen in gastrointestinal surgeries. ![]() The FDA describes that Class I Recalls are reserved for “situations in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death”. (a subsidiary of Johnson & Johnson), for various defects which can increase the risk of severe injury or even death to patients undergoing treatment with the products. On May 15, 2019, the FDA issued a Class 1 Recall for a pair of surgical stapler devices manufactured by Ethicon, Inc. ![]()
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