FDA Adverse Event Malfunction Summary report: N

SUPPORT ARM 177

MDR report key: 1625942 · Received March 3, 2010

Report

Report Number
8010042-2010-00027
Event Type
Malfunction
Date Received
March 3, 2010
Date of Event
January 6, 2010
Report Date
February 8, 2010
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
IOY
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

(B) (4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE SUPPORT ARM HAD A CRACK IN THE JOINT. (B) (4)-(B) (4).

Devices

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

Patients

Seq Age Sex Outcome Treatment
1