Avenir Muller Stem — Class II medical device recall Z-1525-2018
Terminated recall by Zimmer GmbH, reported 2018-05-02. A potential commingle that could result in the product in the package not matching the product on the outer la
| Recall number | Z-1525-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer GmbH, Winterthur, N/A, Switzerland |
| Recall initiated | 2018-02-28 |
| Classified | 2018-04-26 |
| Reported by FDA | 2018-05-02 |
| Terminated | 2019-10-25 |
| Countries outside the US | BE, CH, DE, FR, IT, TH |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00889024479500 |
| Lot numbers | 2905496 |
| Model numbers | 01.06010.104 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1525-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.