Zimmer Biomet recalls Vanguard Knee System Series-A Standard Patella sizes 31mm (Item 184764) due to potential size mismatch with label. Affected patients should contact 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 31mm (Item 1847: 399960) because the implant size might not match the label. This mismatch could lead to improper fitting and complications after surgery.
The implant size might not match the label, which could lead to improper fitting during surgery. This mismatch might cause complications like improper joint function or additional surgical adjustments.
Patients who received the Vanguard Knee System Series-A Standard Patella sizes 31mm (Item 184764) with Lot Number 399960 are affected. Those at highest risk are patients who have recently had knee surgery with this specific implant.
Check for the product name 'Vanguard Knee System Series-A Standard Patella', size 31mm, Item Number 184764, Lot Number 399960, and UDI Number (01)00880304431317(17)230302(10)399960.
Reach out to Zimmer Biomet directly for specific guidance on the recalled product.
The recall is for potential size mismatch with the label, which could lead to improper fitting. However, the hazard is not described as causing serious injury, so it's considered low risk.
Check for the product name 'Vanguard Knee System Series-A Standard Patella', size 31mm, Item Number 184764, Lot Number 399960, and UDI Number (01)00880304431317(17)230302(10)399960.
Contact Zimmer Biomet directly for specific guidance on the recalled product.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0937-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0937-2019 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.
