McKesson 241Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10612479205892), received between Jan 7, 2026 and Apr 8, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Difficult to Remove” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryApr 8, 2026Difficult to Remove

  IT WAS REPORTED BY THE CUSTOMER THAT WHEN ATTEMPTING TO REMOVE STAPLE, THE PLIERS CRIMPED THE STAPLE AND PUSHED IT DOWNWARD INTO THE SKIN INSTEAD OF LIFTING IT OUTWARD. PATIENT DID HAVE TO GO INTO SURGEON'S OFFICE TO GET THE STAPLES REMOVED AFTER THEY BECAME BOWED AND REMAINED IN THE SKIN.

  Patient problems: Skin Tears

  MAUDE report 24813881 ↗
• InjuryJan 7, 2026Difficult to Remove

  IT WAS REPORTED BY THE CUSTOMER THAT WHEN ATTEMPTING TO REMOVE STAPLE, THE PLIERS CRIMPED THE STAPLE AND PUSHED IT DOWNWARD INTO THE SKIN INSTEAD OF LIFTING IT OUTWARD. PATIENT DID HAVE TO GO INTO SURGEON'S OFFICE TO GET THE STAPLES REMOVED AFTER THEY BECAME BOWED AND REMAINED IN THE SKIN.

  Patient problems: Skin Tears

  MAUDE report 23990722 ↗