FDA Adverse Event Malfunction Summary report: N

SUPPORT ARM 177

MDR report key: 3110531 · Received April 5, 2013

Report

Report Number
3008355164-2013-00085
Event Type
Malfunction
Date Received
April 5, 2013
Report Date
March 12, 2013
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
IOY
Product Problem
Yes
Report Source
Distributor report
Reporter Location
SZ
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE SUPPORT ARM BROKE. THERE WAS NO PATIENT HARM. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
141675 SUPPORT ARM 177 IOY MAQUET CRITICAL CARE AB NA NA

Patients

Seq Age Sex Outcome Treatment
1 NI