Depuy recalls ATTUNE Revision Hinge Femoral RT SZ 3 CEM parts due to potential sterility compromise from packaging adhesion. Affected units have specific part numbers and expiration dates.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Depuy is recalling a specific hip implant part because the sterile packaging might stick to the inside packaging, risking infection during surgery. This affects patients who received this part in procedures after the specified date.
The external sterile packaging can stick to the internal sterile packaging, which might compromise the sterility of the implant part. This could lead to infection if the part is used in surgery without proper sterility.
Patients who received the ATTUNE Revision Hinge Femoral RT SZ 3 CEM implant part during surgery between 2023 and 2035 are affected. Surgeons and hospitals using this part are most at risk.
Check for part number 150450203 on the packaging. The expiration date is 10/31/2035, and the lot number is 1007537. This part was sold between 2023 and 2035.
Look for part number 150450203, lot number 1007537, and expiration date 10/31/2035 on the packaging.
Yes, this is a hip implant part used in revision surgeries.
The recall does not specify a remedy, so contact Depuy directly for guidance.
The lot number 1007537 indicates production between 2023 and 2035.
We’ve drafted a message you can send Depuy to request your refund or repair — edit it as you like.
Subject: Recall Z-1989-2026 — Depuy Depuy Hello, I own a Depuy that is covered by recall Z-1989-2026 from Depuy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.