DePuy recalls ATTUNE Revision Distal Femoral Augment SZ 6 4MM for possible adhesive residue causing soft tissue irritation or infection during knee surgery.
May have adhesive residue on the posterior surface of the femoral augment, if undetected prior to implantation, soft tissue irritation and/or infection may occur.
DeP: ATTUNE Revision Distal Femoral Augment SZ 6 4MM is recalled because adhesive residue may cause soft tissue irritation or infection if not detected before surgery. This affects patients undergoing TKA revision procedures.
If adhesive residue remains on the implant's posterior surface after surgery, it can irritate soft tissues or lead to infection. This risk occurs if the residue wasn't detected before implantation.
Patients who received this specific knee implant component during TKA revision surgery are affected. Surgeons and medical staff using this product for procedures are at risk of complications.
Check for product number 154706001 and lot number JJ3389 on the implant packaging. This component is used in TKA revision surgeries and sold under the ATTUNE brand.
Verify the product number (154706001) and lot number (JJ3389) on the implant packaging.
The recall states that adhesive residue may cause issues if undetected before implantation, but the implant itself is safe when properly prepared.
Look for product number 154706001 and lot number JJ3389 on the implant packaging.
The recall does not require stopping use; it focuses on checking for adhesive residue before implantation.
We’ve drafted a message you can send DePuy to request your refund or repair — edit it as you like.
Subject: Recall Z-0632-2022 — DePuy DePuy Hello, I own a DePuy that is covered by recall Z-0632-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
