FDA Device recall Z-1525-2018
Avenir Muller Stem
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of Avenir Muller Stem by Zimmer, citing A potential commingle that could result in the product in the package not matching the product on the outer label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1525-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-28 |
| Published | 2018-05-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer |
| Distribution | n/a |
Product
Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496
Reason
A potential commingle that could result in the product in the package not matching the product on the outer label.
Identifiers
| code_info | Lot Number: 2905496 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1525-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.