Biomet recalls specific Vanguard Knee System PS Open Box Femoral implants due to incorrect labeling of size and side. Affected items may be misused during knee replacement surgery.
Components Incorrectly labeled as either smaller or larger and incorrect side (right/left).
Biomet is recalling certain Vanguard Knee System PS Open Box Femoral implants because they are incorrectly labeled as either smaller or larger sizes and the wrong side (left/right). This could lead to improper surgical fitting if used without verification.
The implants have incorrect size or side labels, which could cause improper surgical fitting if used without verification. This might lead to complications during knee replacement procedures if the wrong implant is installed.
Patients scheduled for knee joint replacement surgery who received these specific implant models. Surgeons and medical facilities using the recalled items are most at risk of incorrect implant application.
Check for the specific model numbers: 183122 (57.5mm), 183124 (60mm), or 183126 (62.5mm). Look for the UDI codes and lot numbers listed in the recall notice.
Check the model number and size on the implant packaging to confirm if it matches the recalled items (183122, 183124, or 183126).
The recall includes Vanguard Knee System PS Open Box Femoral implants with sizes 57.5 mm (model 183122), 60 mm (model 183124), and 62.5 mm (model 183126).
Check the model number on the implant packaging. If it is 183122, 183124, or 183126, it is part of the recall.
Verify the product details to confirm if it matches the recalled models. If it does, contact Biomet for further instructions.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1043-2023 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-1043-2023 from Biomet. 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.
