DEPUY (IRELAND)

Frequent Recalls

9

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-05-06 to 2026-05-06

Date	Source	Product	Brand	Severity	Units
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.	DEPUY (IRELAND)	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.	DEPUY (IRELAND)	Class II	N/A