CLICKLINE 30310MWSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551121856), received between Jan 2, 2025 and Jan 2, 2025 — classified as 1 injury.

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.

• InjuryJan 2, 2025Break; Corroded; Material Fragmentation; Detachment of Device or Device Component; Break; Corroded; Material Fragmentation; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING THE SURGERY ON A CHILD, THE SCISSORS CAME APART AND ONE OF THE JAWS SEPARATED FROM THE INSTRUMENT. THE SCISSOR JAW WAS RETRIEVED BUT THE LUG THAT HOLDS THE JAW TO THE MAIN INSTRUMENT WAS LOST. PATIENT WAS X RAYED BY C ARM ON THE TABLE, BUT NO LUGS WAS SEEN. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. THE PROCEDURE COULD BE COMPLETED SUCCESSFULLY WITH A DELAY OF LESS THAN 15 MINS. SINCE AN X-RAY WAS DONE AND THE LOCATION OF THE LUG IS UNCLEAR, THIS CASE IS REPORTABLE.

  Patient problems: Unintended Radiation Exposure

  MAUDE report 21060523 ↗