BioPro, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0691-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198

Product Classification:

Class II

Date Initiated: February 1, 2022

Date Posted: March 9, 2022

Recall Number: Z-0691-2022

Event ID: 89605

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.

Status: Terminated

Product Quantity:

Code Information:

Lot Number: 125651; UDI: M20917198

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated