WebSep 3, 2024 · Ethicon is the manufacturer of surgical staples used in procedures such as gastric bypass surgery. A staple recall occurs when a medical device is deemed to have significant risks of serious or even fatal consequences if it is used. A staple recall can involve any part of the manufacturing process from raw materials to finished products. WebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI).
Ethicon® Surgical Stapler Recall Lawsuits What You Must Know
WebEthicon Endo-Surgery Alicia Butler Senior Regulatory Affairs Specialist 475 Calle C Guaynabo, PR 00969 ... Surgical Stapler with Implantable Staples Classification Name: Implantable staple ... These predicates have not been Subjected to a recall related to these design modifications. Ethicon Endo-Surgery, LLC 510(k) ... WebEthicon, a Johnson & Johnson subsidiary, has been subject to multiple surgical stapler recalls over concern of surgical staple injury. Several cases of reported surgical staple injury prompted the FDA in October 2024 to announce a Class I recall of several Ethicon surgical staplers. head on accident liability
Surgical Stapler Lawyer for Claims Against Ethicon Searcy Denney
WebSep 3, 2024 · Ethicon is conducting a surgical staple recall due to a potential failure of certain surgical staples it manufactures. This fault can cause failure to properly close … WebMar 15, 2024 · In May, the FDA issued a Class 1 Recall (the most serious) for the Ethicon® Endo-Surgery Curved Intraluminal Staplers -- due to alarmingly high-rates of reported … WebThe Ethicon surgical stapler recall was issued on April 11, 2024, affecting devices that had been manufactured between March 2024 and March 2024—about 100,000 devices in all. Another recall was initiated by Ethicon in October 2024 due to problems with their Echelon staplers that resulted in malformed staples. head on accident michigan