inforMED
MalfunctionKDP

OHMEDA INTERMITTENT SUCTION UNIT

Received Aug 5, 2011 · Event occurred Aug 2, 2011

Report MW5021681 · MDR key 2202194

Device

Generic name

Regulator

Manufacturer

Ohmeda Medical

Product problems

  • Increase in Suction

Patient

8 DA

  • Irritation
  • Blood Loss

Narrative

Description of Event or Problem

RN CHECKED REGULATOR ON SUCTIONING DEVICE PRIOR TO SUCTIONING INFANT. SETTING WAS TO BE NO HIGHER THAN 60. REGULATOR AT THAT TIME WAS AT THE CORRECT SETTING. RN BEGAN ETT SUCTIONING AND NOTICED BRIGHT RED BLOOD. SHE DISCONTINUED USE AND CHECKED THE SETTING ON THE SUCTION DEVICE AND DISCOVERED THAT THE SUCTIONING REGULATOR HAD JUMPED TO FULL VAC.