LINK Endo-Model Modular Knee Prosthesis System Femoral Segment — Class II medical device recall Z-2049-2023
Ongoing recall by Waldemar Link GmbH & Co. KG (Mfg Site), reported 2023-07-05, distributed in AL, GA, IL, IN, KS, NJ, NY, TX. The firm discovered through customer complaints that device segments may not meet specifications.
| Recall number | Z-2049-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Waldemar Link GmbH & Co. KG (Mfg Site), Norderstedt, N/A, Germany |
| Recall initiated | 2021-03-18 |
| Classified | 2023-06-30 |
| Reported by FDA | 2023-07-05 |
| Distributed | AL, GA, IL, IN, KS, NJ, NY, TX |
| Countries outside the US | AR, AT, AU, BR, DE, ES, FI, FR, GB, IN, IT |
| Quantity | 13 units |
| UPC / GTIN / UDI-DI | 04026575328109 |
| Model numbers | 15-2979/02 |
Product
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left
Reason for recall
The firm discovered through customer complaints that device segments may not meet specifications.
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-2049-2023. 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.