MTP Plate, Left MFP 401Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840118111300), received between Jun 23, 2021 and Jun 23, 2021 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (K131657); they may or may not involve this specific model.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• InjuryJun 23, 2021Fracture; Fracture

  THE EVENT INCLUDED THE FRACTURING OF AN IMPLANTED MTP PLATE AT THE COMPRESSION SLOT AFTER BEING IMPLANTED FOR 105 DAYS. THE AFFECTED HARDWARE WAS ABLE TO BE FULLY REMOVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12053329 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K131657. One submission often covers many models, so check the product and lot details in each record.

• Z-1314-2015 · Feb 16, 2015 · Terminated
  Variable Angle Locking Peg, D:1.8mm x L:14.0mm; Variable Angle Locking Peg, D:1.8mm x L:16.0mm, Variable Angle Locking Peg, D:1.8mm x L:18.0mm; Variable Angle Locking Peg, D:1.8mm