# FDA recall Z-0682-2022

> **BioPro, Inc.** · Class II · device recall initiated 2022-02-01.

## Product

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813

## 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.

## Distribution

US Nationwide distribution in the states of CT, KY, NM, PA, TN, and SD.

## Key facts

- **Recall number:** Z-0682-2022
- **Recalling firm:** BioPro, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-01
- **Report date:** 2022-03-09
- **Termination date:** 2024-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Port Huron, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0682-2022

## Citation

> AI Analytics. FDA recall Z-0682-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0682-2022. Source: US FDA. Licensed CC0.

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