Z-1525-2018 Class II Terminated
FDA device recall Z-1525-2018 was initiated by Zimmer GmbH on Feb 28, 2018 and is designated Class II. Reason for recall: A potential commingle that could result in the product in the package not matching the product on the outer label. The recall status is terminated (terminated Oct 25, 2019).
Recall Details
- Product Type
- Devices
- Report Date
- May 2, 2018
- Initiation Date
- Feb 28, 2018
- Termination Date
- Oct 25, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496
Reason for Recall
A potential commingle that could result in the product in the package not matching the product on the outer label.
Distribution Pattern
There was no distribution to the US. The distribution occurred to the following countries: Belgium, Switzerland, Germany, France, Canary Islands, Italy, and Thailand.
Code Information
Lot Number: 2905496
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1525-2018
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026