NA 309.280Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982185709), received between Oct 15, 2019 and Oct 15, 2019 — classified as 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 15, 2019Break; Break

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED ON AN UNKNOWN DATE THAT INSTRUMENTS WERE FOUND BROKEN IN INSPECTION TIME. THERE IS NO PATIENT CONSEQUENCES. THIS IS REPORT FOR 2 OF 09 OF (B)(4).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9192450 ↗