AVID Medical, Inc. recalls GYN LAPAROSCOPY/LAPAROTOMY
- Recalling company
- AVID Medical, Inc.
- Product
- GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;
- Reason
- Product may be potentially contaminated with a lubricant used during the manufacturing process.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 10, 2026
- Reported
- Oct 14, 2026
- Distribution
- US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
- Status
- Ongoing
- Quantity
- 134
- Lot / codes
- 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;
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0093-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0093-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.