inforMED
MalfunctionDTL

MEDLINE

Received May 28, 2026 · Event occurred Apr 30, 2026

Report 3015910259-2026-00127 · MDR key 25326128

Device

Generic name

Mmii,mp,3v,200s,rh,off,oem

Catalog number

80038301

Lot number

0000138736

Product problems

  • Connection Problem

Patient

Not reported

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

IT WAS REPORTED THAT DURING URGENT CASE STEMI, THE INJECTIONS SYRINGE COMING OFF FROM THE MANIFOLD X 2. HAVE NOTICED WHEN IT IS DRY THE PROBLEM (SPINNING OFF) DOES NOT OCCUR. 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

DURING URGENT CASE STEMI, THE INJECTIONS SYRINGE COMING OFF FROM THE MANIFOLD X 2. HAVE NOTICED WHEN IT IS DRY THE PROBLEM (SPINNING OFF) DOES NOT OCCUR.