n.a. 27050SLRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551232910), received between Jul 26, 2024 and Jul 26, 2024 — 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.

• MalfunctionJul 26, 2024Break; Mechanical Problem; Detachment of Device or Device Component; Break; Mechanical Problem; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING THE UTERINE SEPTAL RESECTION MANEUVER AN INSTRUMENT FRAGMENT DETACHED AND WAS RECOVERED INSIDE THE UTERINE CAVITY. UPON EXTRACTION OF THE INSTRUMENT, IT WAS REALIZED THAT THE PROXIMAL PART HAD DESOLDERE. NO NEGATIVE IMPACT ON THE STATE OF HEALTH OF THE PATIENT REPORTED.

  Patient problems: Foreign Body In Patient; Insufficient Information

  MAUDE report 19840502 ↗