Peri-Loc 71865036Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010641335), received between Dec 6, 2019 and Dec 6, 2019 — classified as 1 malfunction.

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

• MalfunctionDec 6, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT DURING SURGERY, THE SCREW COULDN'T BE REMOVED MANUALLY FROM THE PLATE. THE EVENT CAUSED 45 MINUTES DELAY OF SURGERY.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9426061 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K083032, K210837. 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