PERI-LOC VLP 72800306Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010603050), received between Nov 13, 2017 and Nov 13, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Incomplete or Missing Packaging” (1 report).

1 other recall cover devices cleared under the same FDA submission (K062216, 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryNov 13, 2017Incomplete or Missing Packaging; Incomplete or Missing Packaging

  IT WAS REPORTED THAT DURING THE SURGERY THERE WAS A DELAY OF 40 MIN DUE TO NO PHYSICAL DEVICE ONCE THE PACKAGE WAS OPENED.

  Patient problems: No Information

  MAUDE report 7025803 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K062216, K210837, K213126. 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