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DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
Recalled May 6, 2026 · FDA recall Z-1987-2026 · DEPUY (IRELAND)
Hazard
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. · FDA Class II
Units
3 units
Sold at
US Nationwide distribution in the states of MN, NC, TX.
Description
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
Manufacturer(s)
DEPUY (IRELAND)
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →