Class II
Medical Device Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
DEPUY (IRELAND) · April 3, 2026
Reason for Recall
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Distribution
US Nationwide distribution in the states of MN, NC, TX.
States Affected
NATIONWIDE
Quantity Affected
3 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1987-2026
Status: ongoing
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