Peri-Loc 71800108Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010520074), received between Jun 6, 2022 and Jun 17, 2022 — classified as 2 injuries.

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

1 other recall cover devices cleared under the same FDA submission (K092015, 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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 17, 2022Malposition of Device; Malposition of Device

  IT WAS REPORTED THAT, AFTER AN INTERNAL FIXATION SURGERY PERFORMED ON (B)(6) 2021 ON (B)(6) 2021 THE 4.5MM LAT DIST FEMUR LCK PL 8H R 193MM AND FOUR PROXIMAL SCREWS WERE REPOSITIONED. ON (B)(6) 2022 PATIENT UNDERWENT A REVISION SURGERY DUE TO 4.5MM LAT DIST FEMUR LCK PL 8H R 193MM FRACTURE.

  Patient problems: Insufficient Information

  MAUDE report 14738321 ↗
• InjuryJun 6, 2022Fracture; Fracture

  IT WAS REPORTED THAT, AFTER AN INTERNAL FIXATION SURGERY PERFORMED ON (B)(6) 2021, ON (B)(6) 2021 THE 4.5MM LAT DIST FEMUR LCK PL 8H R 193MM WAS REPOSITIONED. ON (B)(6) 2022 X RAYS SHOWED THAT THE 4.5MM LAT DIST FEMUR LCK PL 8H R 193MM WAS FRACTURED AND ON (B)(6) 2022 THE 4.5MM LAT DIST FEMUR LCK PL 8H R 193MM WAS REMOVED AND EXCHANGED. THE CURRENT HEALTH STATUS OF THE PATIENT IS UNKNOWN.

  Patient problems: Insufficient Information

  MAUDE report 14605599 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K092015, K210837, K213126. One submission often covers many models, so check the product and lot details in each record.

• Z-2036-2017 · Mar 22, 2017 · Terminated
  PERI-LOC VOLAR DISTAL RADIUS - RIGHT 3H STD HEAD LOCKING PLATE, 62 MM LENGTH, SST PLATE, REF 71823114, QTY: (1) NON-STERILE, Rx only, Smith & nephew, Inc., Memphis TN 38116