Depuy recalls ATTUNE Revision Hinge Knee Insert Components with specific part numbers and lot numbers due to potential sterility compromise in packaging.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Depuy is recalling ATTUNE Revision Hinge Knee Insert Components with specific part numbers and lot numbers. The issue involves external sterile packaging adhering to internal sterile packaging, which could compromise sterility during surgical procedures.
The external sterile packaging was found adhered to the internal sterile packaging, which could compromise sterility during surgical procedures. This risk may lead to infections if the components are used without proper sterility.
Patients who have received these knee implant components during surgery are affected. Surgeons and medical facilities using the recalled components are at risk of potential sterility compromise.
Check the product description and part numbers listed in the recall notice. The affected components include specific sizes (4mm to 26mm) with part numbers starting with 151730408 to 151730826 and associated lot numbers.
Review the part numbers and lot numbers listed in the recall notice to determine if your components are affected.
Yes, these are ATTUNE Revision Hinge Knee Insert Components used in knee surgeries.
Check the part numbers and lot numbers listed in the recall notice. Affected components have specific part numbers starting with 151730408 to 151730826 and associated lot numbers.
Review the part numbers and lot numbers to determine if your components are affected. If affected, contact Depuy for further instructions.
We’ve drafted a message you can send Depuy to request your refund or repair — edit it as you like.
Subject: Recall Z-2617-2026 — Depuy Depuy Hello, I own a Depuy that is covered by recall Z-2617-2026 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.
