Foot Plates MTPL-9Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188119989), received between Apr 12, 2022 and Apr 12, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 12, 2022Fracture; Fracture

  A TRIMED SALES REPRESENTATIVE REPORTED ON (B)(6) 2022 THAT A MTPL-9 HAD BROKEN IN THE PATIENT. IT WAS STATED THAT THE SURGEON HAD A (B)(6) PATIENT WHO HAD A PREVIOUSLY FAILED TOE IMPLANT (NOT A TRIMED PRODUCT), THE SURGEON REMOVED THE SILASTIC IMPLANT AND PUT AN ALLOGRAFT BONE WEDGE IN AND PLATED WITH THE MTPL-9. IT WAS STATED BY THE SALES REP AND SURGEON THAT THE FRACTURE LOOKED FUSED AND WAS DOING WELL WHEN THERE WAS A SUDDEN ONSET OF PAIN 3 MONTHS POST SURGERY (INITIAL SURGERY DATE UNKNOWN), IT WAS ALSO MENTIONED THAT THE PATIENT TYPICALLY HAS SURGERY COMPLICATIONS. LASTLY, IT WAS STATED THAT THE SURGEON PLANS TO REMOVE THE HARDWARE, THE SURGERY DATE IS CURRENTLY UNKNOWN. THE SURGEON DOES NOT BELIEVE THAT THIS ISSUE WILL CAUSE ANY LASTING ISSUES IN THE PATIENT.

  Patient problems: Insufficient Information

  MAUDE report 14084240 ↗