Knee Recall: Depuy Synthes ATTUNE Revision Hinge RT 4
Announced 2026-07-08 · FDA
Recall involves Depuy Synthes ATTUNE Revision Hinge knee hinge insert components. External sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. Three units were distributed nationwide in Minnesota, North Carolina, and Texas.
| Brand | DEPUY (IRELAND) |
|---|---|
| Product | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204. |
| Reason | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. |
| Severity | moderate |
| Units affected | 160 |
| Distribution | US Nationwide distribution in the states of MN, NC, TX. |
| Agency | FDA |
| Recall / campaign no. | Part Number: 150450204. UDI-DI: 10603295533153. Lot Number: 1005229. Expiration Date: 10/31/2035. |
WHAT YOU SHOULD DO
- If you were implanted with this device, contact your surgeon or health-care provider to discuss the recall and any needed follow-up.
- If you are a health-care professional with stock of these components, follow your facility's recall procedures and contact the manufacturer or distributor for guidance.
- Check the FDA recall notice or the manufacturer for the latest updates and keep your recall information (lot number 1005229 and Part Number 150450204) handy.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.