GYN LAPAROSCOPY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIOngoing
Summary: AVID Medical, Inc. is recalling GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12;. Reason: Product may be potentially contaminated with a lubricant used during the manufacturing process.
What is being recalled
GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12;
Why
Product may be potentially contaminated with a lubricant used during the manufacturing process.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX. (states named: Arizona, California, Florida, Maryland, Nebraska, Texas)
How to tell if yours is affected
Model/Item Number (Kit): NAMC436-12; UDI-DI: 10809160468470; Kit Lot Numbers: 1697826; Recalled Supplier Component (in kit): A119216M; Recalled Supplier Lot Number (in kit): NGKT3314;
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-0105-2027 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | August 10, 2026 |
| Reported | October 14, 2026 |
| Company | AVID Medical, Inc. |
| Company location | Toano, VA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 28 |
More recalls from AVID Medical, Inc. · all medical device recalls · recalls from August 2026