DePuy recalls specific lots of ATTUNE Rotating Platform total knee implants due to potential damaged packaging. Affected tibial bases may be used in cemented knee replacements. Consumers should check product codes and lots for recall.
Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+) Tibial Bases due to potential damaged packaging. These implant components are utilized in Total Knee Arthroplasty. The affected tibial bases are designed to be used in cemented applications.
DePuy is recalling certain lots of ATTUNE Rotating Platform total knee implants because the packaging might be damaged. This could affect the safety of the implant during surgery. Patients with these specific product codes should contact DePuy for details.
The recall is for potential damaged packaging in the tibial bases used in cemented knee replacements. Damaged packaging could lead to improper handling or installation during surgery, though the hazard is not described as causing immediate injury.
Patients who received the ATTUNE Rotating Platform total knee implant system with the listed product codes and lots are affected. Surgeons and medical facilities using these specific components are at risk.
Check your implant's product code (150680003-150680007) and lot numbers (9556100-9557476) on the packaging. The recall covers specific lots of tibial bases used in cemented knee replacements.
Look for the product code (150680003-150680007) and lot numbers (9556100-9557476) on the implant packaging.
The recall is for potential damaged packaging in the tibial bases used in cemented knee replacements, which could affect surgical installation.
No, the recall does not require stopping use. The hazard is potential packaging damage, not an immediate safety risk during normal use.
Check your implant's product code (150680003-150680007) and lot number (9556100-9557476) on the packaging.
We’ve drafted a message you can send DePuy to request your refund or repair — edit it as you like.
Subject: Recall Z-1316-2021 — DePuy DePuy Hello, I own a DePuy that is covered by recall Z-1316-2021 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.
