Notice names this product. AVID Medical’s UROLOGY MAJOR is named in FDA Class II recall Z-0103-2027.
Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies.Agency-reported hazard: Product may be potentially contaminated with a lubricant used during the manufacturing process. Identifying details: Model/Item Number (Kit): WRNM058-10; UDI-DI: 10809160488898; Kit Lot Numbers: 1681989; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU2887;. Units affected: 20. Status: Ongoing.
1. Compare your item
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Product named
UROLOGY MAJOR
Company / brand
AVID Medical
Lot / serial / date codes
Model/Item Number (Kit): WRNM058-10; UDI-DI: 10809160488898; Kit Lot Numbers: 1681989; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU2887;
Distribution
US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
Agency product description and boundaries
UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.