Peri-Loc 71860106Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010640161), received between Jan 4, 2021 and Jan 4, 2021 — classified as 1 injury.

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

2 other recalls cover devices cleared under the same FDA submission (K083032, K210837, K213126); 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.

• InjuryJan 4, 2021Break; Break

  IT WAS REPORTED THAT, THERE WAS A REVISION SURGERY DUE TO PERI-LOC 4.5MM TITANIUM L-D FEM PL 8H R 193MM BREAKAGE, THIS DEVICE WAS EXPLANTED. THE PROCEDURE WAS COMPLETED WITH A COMPETITOR DEVICE (STRYKER PLATE). NO SURGICAL DELAY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11113376 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K083032, K210837, K213126. One submission often covers many models, so check the product and lot details in each record.

• Z-0372-2016 · Oct 20, 2015 · Terminated
  Smith & Nephew PERI-LOC VOLAR DISTAL RADIUS PLATE STANDARD 3 HOLE SHORT, LEFT - 62 MM, STERILE R, Rx only, REF Numbers: 71863110 Bone fixation plate
• Z-0373-2016 · Oct 20, 2015 · Terminated
  Smith & Nephew PERI-LOC VOLAR DISTAL RADIUS PLATE STANDARD 3 HOLE SHORT, RIGHT - 62 MM, STERILE R, Rx only, REF Numbers: 71863114 Bone fixation plate