Peri-Loc 71800010Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010520029), received between Apr 4, 2017 and Jan 27, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Break” (2 reports).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJan 27, 2022Fracture; Fracture

  IT IS REPORTED THAT, AFTER AN INTERNAL FIXATION SURGERY WAS PERFORMED ON (B)(6) 2021, THE PATIENT ATTENDED THE HOSPITAL BECAUSE OF PAIN AND DEFORMITY. AFTER EVALUATION, IT WAS FOUND THAT THE 4.5MM L-D FEM LK PL10H L 230MM IS BROKEN. A REVISION SURGERY HAS NOT BEEN PERFORMED.

  Patient problems: Deformity/ Disfigurement; Failure of Implant; Pain

  MAUDE report 13364852 ↗
• InjuryJul 24, 2018Break

  IT WAS REPORTED THE BROKEN PLATE WAS REMOVED FROM A PATIENT BY (B)(6)HOSPITAL. THE PLATE WAS ORIGINALLY INSTALLED BY A SURGEON IN A HOSPITAL IN (B)(6). THE DATE OF THE ORIGINAL SURGERY IS UNKNOWN AS IS THE NAME OF THE HOSPITAL AND SURGEON.

  Patient problems: Failure of Implant

  MAUDE report 7713569 ↗
• InjuryApr 4, 2017Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT FOLLOWING FEMORAL PLATING DUE TO OLD INJURY AND BONE MALUNION, THE PATIENT UNDERWENT REVISION SURGERY DUE TO BROKEN FEMORAL PLATE IMPLANT.

  Patient problems: Failure of Implant

  MAUDE report 6456034 ↗

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