Medline CISION10SSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30193489090127), received between Apr 18, 2025 and Apr 18, 2025 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 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.

• InjuryApr 18, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON 2/27, "THERE WAS SIGNIFICANT RESISTANCE PUSHING THE BLADE OFF THE SCALPEL HOLDER WITH NEEDLE DRIVERS WHILE CLEANING UP POST-SURGERY. ON ONE ATTEMPT, THE BLADE (STILL ATTACHED TO HOLDER) REBOUNDED AFTER PUSHING WITH NEEDLE DRIVERS AND LACERATED THE LATERAL ASPECT OF MY RIGHT THUMB".

  Patient problems: Laceration(s)

  MAUDE report 21866096 ↗