Peri-Loc 71823014Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010526298), received between Apr 13, 2020 and Apr 13, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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

• InjuryApr 13, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT ONCE THE HALLUX WITH PINS WAS REDUCED, THE DOCTOR LOCATED THE LEFT MTP PLATE (72824015) FOLLOWING THE INDICATED SURGICAL TECHNIQUE, LOCATED THE DRILL GUIDE DRILL WITH THE 2.0 DRILL PERPENDICULAR TO THE BONE, MEASURED AND LOCATED THE 2.7 CORTICAL SCREW X14. FOR THE FOLLOWING SCREWS AND USING THE SAME SURGICAL TECHNIQUE BUT WITH THE VARIABLE ANGLE GUIDE, SURGEON PROCEEDED TO PLACE THE LOCKED SCREWS AND NOTED THAT THEY DID NOT LOCK ON THE PLATE, CHANGE MEASUREMENTS, CHANGE DIRECTION AND EVEN SO THEY GAVE INSUFFICIENT FIXATION. FINALLY, SURGEON DECIDED TO PERFORM THE ARTHRODESIS WITH S&N CANNULATED SCREWS, IT IS CLEAR THAT NO PART OF THE IMPLANT REMAINED INSIDE THE PATIENT AND THE PROBLEM COULD BE SATISFACTORILY RESOLVED. THE PATIENT HEALTH CONDITIONS IS STABLE AND NO DAMAGE OCCURRED TO THE PATIENT DUE TO THIS EVENT. DELAY OF (0 30) MINUTES REPORTED.

  Patient problems: Injury

  MAUDE report 9953456 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K033669. 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: