CLICKLINE 33510UMRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551151198), received between Aug 13, 2021 and Aug 13, 2021 — 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.

• MalfunctionAug 13, 2021Break; Break

  AS PER A MANUFACTURER INCIDENT REPORT WE RECEIVED FROM THE FACTORY IN (B)(6): ON 13/07/21 DISTRIBUTOR MADE AWARE THAT THE PART THAT DETACHED FROM THE INSTRUMENT HAS BEEN CONFIRMED TO HAVE BEEN RETAINED INSIDE THE PATIENT AND HAS BEEN DISCOVERED UNDER X-RAY. REVISION SURGERY WILL BE REQUIRED TO REMOVE.

  Patient problems: Foreign Body In Patient

  MAUDE report 12321021 ↗