Official recall notice
FDA DeviceClass IINotable
FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.
- Recall date
- 2026-05-06
- Brand
- DEPUY (IRELAND)
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Recommended action
What to do
3 units
Product description
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.