Invictus 17125Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190376269573), received between Nov 17, 2021 and Nov 17, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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.

• InjuryNov 17, 2021Activation, Positioning or Separation Problem

  DURING SURGERY, THE ROD WOULD NOT PROPERLY LOCK TO THE MIS ROD INSERTER. THERE APPEARED TO BE LACK OF NECESSARY RIGID INTERFACE BETWEEN THE ROD AND INSERTER, WHICH MADE IT DIFFICULT TO PASS AND SEAT THE ROD. THIS CAUSED A DELAY IN SURGERY. NO PATIENT INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12833094 ↗