Medium risk Drugs & MedicationsClass II

DEPUY (IRELAND) Recall

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.

Updated April 3, 2026

DEPUY (IRELAND) is recalling 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.

Is the DEPUY (IRELAND) recalled? Yes. This product was recalled by FDA on April 3, 2026. Details below.

What is recalled

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

Brands affected

Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1988-2026
Classification
Class II
Recalled
April 3, 2026
Read the official notice

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