Exactech recalls OPTETRAK One Peg Patella knee components with out of specification vacuum packaging. Affected items include specific model numbers and lot numbers. Consumers should contact Exactech for details.
Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.
Exactech is recalling certain knee patella components due to vacuum bags that don't meet quality standards. This could lead to improper fitting or damage during surgery if used without proper packaging.
The vacuum bags used to package the knee components are out of specification, meaning they may not hold the components securely during surgery. This could lead to improper fitting or damage if the components are not handled correctly.
Patients who received these specific knee implants during surgery are most at risk. The recall affects individuals with the listed model numbers and lot numbers from the provided list.
Check the item number on the packaging (200-03-26 to 200-03-41) and the lot numbers listed in the recall notice. The affected items include specific sizes and lot numbers provided in the recall details.
Reach out to Exactech directly to confirm if your specific model and lot numbers are affected and to get instructions for replacement or return.
Exactech is recalling these knee components because the vacuum bags used to package them are out of specification, which could lead to improper fitting or damage during surgery.
Check the item number on the packaging (200-03-26 to 200-03-41) and the lot numbers listed in the recall notice. The affected items include specific sizes and lot numbers provided in the recall details.
Contact Exactech directly to confirm if your specific model and lot numbers are affected and to get instructions for replacement or return.
We’ve drafted a message you can send Exactech to request your refund or repair — edit it as you like.
Subject: Recall Z-2156-2024 — Exactech Exactech Hello, I own a Exactech that is covered by recall Z-2156-2024 from Exactech. 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.
