Peri-Loc 71173491Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556016718), received between Dec 5, 2020 and Dec 5, 2020 — classified as 2 injuries.

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

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 5, 2020Material Deformation; Material Deformation

  IT WAS REPORTED DURING THE PROCEDURE THAT THE SURGEON WAS UNABLE TO SCREW INTO THE IMPLANTS, BECAUSE THE THREADS OF DEVICES WERE STRIPPED. ALTHOUGH THE PROCEDURE WAS COMPLETED WITHOUT DELAY, THE SURGEON HAD TO CHANGE THE SURGICAL TECHNIQUE TO FINISHED THE SURGERY. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10950764 ↗
• InjuryDec 5, 2020Material Deformation; Material Deformation

  IT WAS REPORTED DURING THE PROCEDURE THAT THE SURGEON WAS UNABLE TO SCREW INTO THE IMPLANTS, BECAUSE THE THREADS OF DEVICES WERE STRIPPED. ALTHOUGH THE PROCEDURE WAS COMPLETED WITHOUT DELAY, THE SURGEON HAD TO CHANGE THE SURGICAL TECHNIQUE TO FINISH THE SURGERY. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10950743 ↗