DEPUY (IRELAND) recalls Depuy Synthes
- Recalling company
- DEPUY (IRELAND)
- Product
- Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.
- Reason
- The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 3, 2026
- Reported
- May 6, 2026
- Distribution
- US Nationwide distribution in the states of MN, NC, TX.
- Status
- Ongoing
- Quantity
- 3 units
- Lot / codes
- Part Number: 150450104. UDI-DI: 10603295533115. Lot Number: 1007844. Expiration Date: 11/30/2035
- Company location
- Co. Cork
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1985-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1985-2026 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.