Zimmer recalls Avenir Muller Stem Standard size 1 due to mislabeling in packaging. The stem inside packaging is actually size 2, which could lead to improper fit during hip surgery.
Mislabeled Labeled Avenir M¿ller Stem size 1, the stem inside the packaging is an Avenir M¿ller Stem size 2 .
Zimmer is recalling Avenir Muller Stem Standard size 1 implants because the packaging incorrectly labels them as size 1 when they are actually size 2. This mislabeling could cause improper surgical fitting if used without correction.
The stems are mislabeled in the packaging, meaning the product sold as size 1 is actually size 2. This could lead to improper surgical fitting if the implant is used without correction, potentially causing complications during hip replacement procedures.
Patients who received the Avenir Muller Stem Standard size 1 implant during hip surgery are affected. Surgeons and medical facilities using this specific implant model are most at risk.
Check for the product name 'Avenir Muller Stem Standard', item number 01.06010.001, and lot number 2955599. The stems are intended for total or hemi-hip arthroplasty procedures.
Check the item number (01.06010.001) and lot number (2955599) on the packaging to confirm the correct size.
The product is recalled because the packaging mislabels Avenir Muller Stem size 1 as size 1 when it is actually size 2, which could lead to improper surgical fitting.
The recall record does not specify a remedy, so contact Zimmer directly for guidance on next steps.
The recall indicates a potential misfitting risk during hip surgery, but the hazard level is low_risk as the remedy is not specified and the issue is a labeling error.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-0644-2019 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-0644-2019 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.
