Depuy recalls ATTUNE Revision Hinge Femoral LT SZ 7 CEM parts due to potential sterility compromise from packaging adhesion. Affected units have specific part numbers and lot 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 is a serious issue for patients undergoing hip replacement procedures.
The external sterile packaging can stick to the internal sterile packaging, which might compromise the sterility of the implant. If the packaging isn't sterile, it could lead to infection during surgery.
Patients who received this specific hip implant part during surgery are most at risk. Healthcare providers using the part for surgical procedures may also be affected.
Check for part number 150450107, lot number 1006440, and expiration date 11/30/2035 on the packaging. This part was sold by Depuy in Ireland.
Look for part number 150450107, lot number 1006440, and expiration date 11/30/2035 on the packaging.
Yes, this is a hip implant part for revision surgeries.
Check for part number 150450107, lot number 1006440, and expiration date 11/30/2035 on the packaging.
The recall does not specify a stop-use action; the hazard is about potential sterility compromise during surgery.
We’ve drafted a message you can send Depuy to request your refund or repair — edit it as you like.
Subject: Recall Z-1987-2026 — Depuy Depuy Hello, I own a Depuy that is covered by recall Z-1987-2026 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.
