TemporaryFDAOngoing
Can cause harm that is usually temporary.
GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;
Check the device or its packaging for
1. Model/Item Number (Kit): WRNM002-15; UDI-DI: 10809160487181; Kit Lot Numbers: 1666722; 2. Model/Item Number (Kit): FBCH108-03; UDI-DI: 10809160399781; Kit Lot Numbers: 1659079, 1696378; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKU3975, NGKU2887;
- Why
- Product may be potentially contaminated with a lubricant used during the manufacturing process.
- Distributed
- US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
- Company
- AVID Medical, Inc.
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-0093-2027 · retrieved 7 October 2026
Read the official notice