LINK MP Monoblock Hip Stem — Class II medical device recall Z-2351-2023
Ongoing recall by Waldemar Link GmbH & Co. KG (Mfg Site), reported 2023-08-16, distributed nationwide. Increased force may be required to remove the LINK MP Monoblock trial hip stem (Sizes 14mm - 25mm),after impac
| Recall number | Z-2351-2023 |
|---|---|
| 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 | 2023-07-03 |
| Classified | 2023-08-04 |
| Reported by FDA | 2023-08-16 |
| Distributed | Nationwide (US) |
| Quantity | 24 units |
| UPC / GTIN / UDI-DI | 04026575182145 |
| Lot numbers | B922121, B933166, C005012, C211014 |
| Model numbers | 136-120/00 |
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 20 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-120/00
Reason for recall
Increased force may be required to remove the LINK MP Monoblock trial hip stem (Sizes 14mm - 25mm),after impaction. Potential for prolongation of surgery or the surgical procedure may have to be modified due to this issue
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-2351-2023. 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.