Zimmer recalls Avenir Muller Stem (Lot 2905496) due to potential mismatch between product in package and outer label. Consumers should check labels and contact Zimmer for details.
A potential commingle that could result in the product in the package not matching the product on the outer label.
Zimmer is recalling a specific model of Avenir Muller Stem due to a possible mismatch between the product inside the package and the label on the outside. This could lead to confusion about the product's identity, but it does not pose a safety risk.
The product may not match the label on the outside of the package. This could cause confusion about which product is being used, but it does not involve physical harm or safety risks.
Users of the specific Avenir Muller Stem model (Item 01.06010.104) with Lot Number 2905496 are affected. Medical professionals using this product are most at risk of confusion.
Check for the Item Number 01.06010.104 and Lot Number 2905496 on the package. The product was sold with a specific UDI code (01)00889024479500 (17)220430 (10)2905496.
Verify the Item Number and Lot Number on the package to confirm if it matches the recalled model.
No, this recall is about potential label mismatch, not a safety hazard.
Check for Item Number 01.06010.104 and Lot Number 2905496 on the package.
Contact Zimmer directly to confirm if your product is affected.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1525-2018 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1525-2018 from Zimmer. 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.
