DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
- Recall date
- April 3, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1992-2026
- FDA classification
- Class II
- Brand / firm
- DEPUY (IRELAND)
- Sold / distributed
- US Nationwide distribution in the states of MN, NC, TX.
Why it was recalled
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
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