inforMED
MalfunctionGES

MEDLINE

Received Jun 11, 2026 · Event occurred May 14, 2026

Report 1423395-2026-00270 · MDR key 25479798

Device

Generic name

Div22 Preferred Sterile - Miscellaneous

Catalog number

DIV22

Product problems

  • Break

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

IT WAS REPORTED THAT THE BLADE KEPT BREAKING DURING THE CASE. THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS IS A REPORTABLE EVENT. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THIS REPORT WILL BE REOPENED AND REEVALUATED.

Description of Event or Problem

IT WAS REPORTED THAT THE BLADE KEPT BREAKING DURING THE CASE.