FDA Adverse Event Injury Summary report: N

*

MDR report key: 512818 · Received February 11, 2004

Report

Report Number
MW1031140
Event Type
Injury
Date Received
February 11, 2004
Date of Event
February 11, 2004
Report Date
February 11, 2004
Manufacturer
ERIE MEDICAL
Product Code
CAN
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

OXYGEN CYLINDER WAS TURNED ON TO GIVE THE PT OXYGEN. THE NOSE POPPED OFF AND THE REGULATOR EXPLODED. THE PT WAS HIT, BUT FELT MUCH BETTER LATER ON NO SERIOUS INJURIES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * OXYGEN REGULATOR CAN ERIE MEDICAL UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 86 YR