EVOS 71158203Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556693797), received between Jul 10, 2020 and Jul 10, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Defective Device” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 10, 2020Defective Device; Defective Device

  IT WAS REPORTED THAT DURING A WRIST CASE, A LOCKING SCREW PUSHED THROUGH THE 71158203 R 3H STD VOLAR PLATE. THE TABS WERE COMPLETELY GONE AND WERE RETRIEVED OUTSIDE THE PATIENT. DR. USED THE VA GUIDE CORRECTLY AND ONLY DRILLED AT AN APPROPRIATE ANGLE. HE HAD TO SWITCH TO A 4 HOLE PLATE TO FINISH THE CASE WHICH WE HAD AVAILABLE TO HIM. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10258528 ↗