Peri-Loc 71829010Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010525581), received between Jun 20, 2017 and Jun 20, 2017 — 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); 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 20, 2017Fracture; Break; Fracture

  IT WAS REPORTED THAT DURING FOLLOW UP 3/23/17 PATIENT COMPLAINED OF PAIN AND SURGEON NOTICED THE BROKEN PLATE. REVISION SURGERY WAS PERFORMED AND A BROKEN PLATE WAS REMOVED.

  Patient problems: Injury; Pain

  MAUDE report 6652953 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K033669, K210837. 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: