TRIAL STEM for MP — Class II medical device recall Z-2074-2013
Terminated recall by Waldemar Link GmbH & Co. KG (Corp. Hq.), reported 2013-09-04, distributed in TN. The trial stems were manufactured using the wrong design.
| Recall number | Z-2074-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Waldemar Link GmbH & Co. KG (Corp. Hq.), Hamburg, Germany |
| Recall initiated | 2013-07-16 |
| Classified | 2013-08-27 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2014-06-04 |
| Distributed | TN |
| Quantity | 5 units |
| Lot numbers | B208037, B225126 |
| Model numbers | 99-0155/12 |
Product
TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0155/12, Stem size S-0, prox. Stem dia. 12 mm, Length 180 mm, WALDEMAR LINK GmbH & CoKG, Barkhausenweg 10 . D . 22339 Hamburg
Reason for recall
The trial stems were manufactured using the wrong design.
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-2074-2013. 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.