PERI-LOC 71820010Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010527431), received between May 26, 2022 and May 26, 2022 — 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 (K092015, 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.

• InjuryMay 26, 2022Break; Break

  IT WAS REPORTED THAT, DURING SURGERY, A 4.5MM L-D FEM LK PL 10H L 230MM BROKE, IT IS UNKNOWN WHEN THE EVENT HAPPENED (INTERNAL OR EXTERNAL) OR IF THERE WAS ANY DELAY OR INJURY. IT IS UNKNOWN IF THERE WAS A S&N BACKUP DEVICE AVAILABLE.

  Patient problems: Bone Fracture(s); Failure of Implant; No Clinical Signs, Symptoms or Conditions; Nonunion/Delayed-union Bone Fracture; Pain

  MAUDE report 14506036 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K092015, K210837. 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