MobileLink Acetabular Cup System — Class II medical device recall Z-2641-2023
Ongoing recall by Waldemar Link GmbH & Co. KG (Mfg Site), reported 2023-10-04, distributed in AL, NJ, NV. Product is labeled with incorrect offset.
| Recall number | Z-2641-2023 |
|---|---|
| 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 | 2023-07-14 |
| Classified | 2023-09-26 |
| Reported by FDA | 2023-10-04 |
| Distributed | AL, NJ, NV |
| Quantity | 8 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04026575182329 |
| Lot numbers | 210526/0771, 210526/0772, 210526/0777, 210526/0778, 210526/0779, 210526/0781, 210526/0783, 210526/0784 |
| Model numbers | 183-610/05, 210526/0781 |
Product
MobileLink Acetabular Cup System, Shell/Insert Adapter for Shell 74-80mm, Insert Size F, +12mm Offset 20 degrees Inclination
Reason for recall
Product is labeled with incorrect offset.
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-2641-2023. 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.