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DEPUY (IRELAND) Recalls
11 recalls on record · May 6, 2026 to July 8, 2026 · Medical Devices
July 8, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
July 8, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with the below product descriptions and Part Codes.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.