Titanium MPJ — Class II medical device recall Z-0688-2022
Terminated recall by BioPro, Inc., reported 2022-03-09, distributed nationwide. There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP10230
| Recall number | Z-0688-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | BioPro, Inc., Port Huron, MI, United States |
| Recall initiated | 2022-02-01 |
| Classified | 2022-02-28 |
| Reported by FDA | 2022-03-09 |
| Terminated | 2024-02-28 |
| Distributed | Nationwide (US) |
| Lot numbers | 124737, 125470 |
| Model numbers | 17037 |
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
Reason for recall
There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
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-0688-2022. 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.