FDA Adverse Event Injury Summary report: N

LAERDAL AIRWAY LUBRICANT (LAL)

MDR report key: 561120 · Received May 10, 2004

Report

Report Number
9610483-2004-00004
Event Type
Injury
Date Received
May 10, 2004
Report Date
April 13, 2004
Manufacturer
LAERDAL MEDICAL A/S
Product Code
BSJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

A PT CLAIMS TO HAVE INCURRED ALLEGED DEBILITATING INJURY FOLLOWING AN ALLEGED PHYSICAL REACTION UPON ALLEGED "EXPOSURE" TO LAERDAL AIRWAY LUBRICANT (LAL) THAT WAS SPRAYED ONTO THE NASAL TUBE DURING THE TRAINING SCENARIO. IT WAS DETERMINED THE CO2 POWERED GLYCEROL LAL, ITEM# 071400, MAY HAVE BEEN THE PRODUCT IN USE AT THE TIME OF THE ALLEGED INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LAERDAL AIRWAY LUBRICANT (LAL) SPRAY LUBRICANT BSJ LAERDAL MEDICAL A/S NA UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN