EVOS 71175025Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556635810), received between Oct 3, 2018 and Aug 19, 2020 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

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.

• MalfunctionAug 19, 2020Break; Material Twisted/Bent; Break; Material Twisted/Bent

  IT WAS REPORTED THAT DURING A TRAUMA SURGERY, EXTERNAL TO PATIENT, THE EVOS SMALL 2.7MM OVERDRILL W/AO QC SHORT BROKE AT CONNECTION AND BENT AT TIP. THE PROCEDURE WAS FINISHED USING A SMITH AND NEPHEW BACK UP DEVICE, WITH NO SURGICAL DELAY AND NO INJURY TO THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10428103 ↗
• InjuryOct 3, 2018Connection Problem; Connection Problem

  DRILL GOT STUCK IN DRILL GUIDE, ON REMOVAL, THIS HIT THE SCRUB NURSE ON THE HAND AND PULLED THE MEDICAL FRAGMENT FROM THE BONE OF THE PATIENT.

  Patient problems: No Information

  MAUDE report 7931236 ↗