Zimmer Biomet recalls Vanguard Knee System Series-A Standard Patella 34mm implants with potential size mismatch. Affected units have specific lot numbers and item numbers. Consumers should contact Zimmer Biomet for details.
Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.
Zimmer Biomet is recalling Vanguard Knee System Series-A Standard Patella sizes 34mm due to a potential size mismatch between the implant and label. This mismatch could lead to improper fit during surgery, affecting the procedure's safety and effectiveness.
The implant size may not match the label, which could lead to improper surgical fit. This mismatch might cause complications during knee replacement surgery, such as incorrect alignment or tissue damage.
Patients who received the Vanguard Knee System Series-A Standard Patella 34mm implant with specific lot numbers (38180: 381800 and 400030) are affected. Surgeons and medical staff who used these implants during procedures are at higher risk.
Check for the item number 184766 and lot numbers 381800 or 400030 on the implant packaging or documentation. The UDI number starts with (01)00880304434349.
Reach out to Zimmer Biomet directly for specific details about your implant and next steps.
The recalled implant is the Vanguard Knee System Series-A Standard Patella size 34mm with item number 184766.
Check for the item number 184766 and lot numbers 381800 or 400030 on the implant packaging or documentation.
The recall does not require immediate discontinuation; contact Zimmer Biomet for specific guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0938-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0938-2019 from Zimmer 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.
