inforMED
InjuryBTA

LAERDAL V-VAC

Received Sep 20, 2022 · Event occurred Jul 27, 2022

Report MW5112156 · MDR key 15462217

Device

Generic name

Pump, Portable, Aspiration (manual Or Powered)

Model number

J52

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

57 YR · Male

  • Hemorrhage/Blood Loss/Bleeding
  • Hemorrhage/Blood Loss/Bleeding

Narrative

Description of Event or Problem

NASAL BLEEDING. FDA SAFETY REPORT ID# (B)(4).