Peri-Loc 71829457Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010527691), received between Nov 23, 2020 and Nov 23, 2020 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (K033669, 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.

• InjuryNov 23, 2020Break; Break

  IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO THE PLATE USED TO TREAT PATIENT'S HUMERAL FRACTURE HAD BROKEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10884202 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K033669, K210837, K213126. One submission often covers many models, so check the product and lot details in each record.

• Z-2314-2010 · Jul 20, 2010 · Terminated
  PERI-LOC (R), 3.5 MM ANTEROLATERAL DISTAL TIBIA PLATE, 10 HOLE, RIGHT - 148 MM, REF 71800710, QTY: (1), STERILE R, CE 0086, Smith & Nephew, Inc., Memphis, TN 38116, USA, EC REP: