PERI-LOC VLP 72820207Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556067062), received between Jun 28, 2018 and Jun 28, 2018 — 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 (K062216, 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 18, 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 28, 2018Break; Break

  IT WAS REPORTED THAT A SURGICAL INTERVENTION WAS PERFORMED DUE TO A BROKEN PLATE. THE PLATE WAS REMOVED.

  Patient problems: No Information

  MAUDE report 7648779 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K062216, K210837. One submission often covers many models, so check the product and lot details in each record.

• Z-1854-2017 · Mar 9, 2017 · Terminated
  Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic