NA 702876Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540413895), received between Dec 3, 2018 and Dec 3, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect Measurement” (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.

• MalfunctionDec 3, 2018Incorrect Measurement

  DURING PELVIC SURGERY THE LONG INNER PORT OF 702877 WAS INSERTED IN THE OUTER PORT OF 702876 WHICH RESULTED IN A TOO LONG MEASUREMENT. DURING INSERTION OF THE SCREW THE MISTAKE WAS DETECTED. CUSTOMER STATED THAT THERE IS NO NUMBER ON THE INNER PORT TO VERIFY WHICH PORTS OF THE 2 DEVICES BELONG TOGETHER. SURGICAL DELAY OF 5 MIN. NOT LONGER. NO OTHER CONSEQUENCES REPORTED. THE CUSTOMER STATED THAT THERE IS A POSSIBILITY OF HAZARD IF WRONG MEASUREMENT IS NOT DETECTED. IN THIS CASE PATIENT WAS NOT HARMED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8126098 ↗