FDA Adverse Event Malfunction Summary report: N

SUPPORT ARM 176

MDR report key: 3142281 · Received May 21, 2013

Report

Report Number
8010042-2013-00079
Event Type
Malfunction
Date Received
May 21, 2013
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
IOY
PMA / PMN Number
NA
Report Source
Manufacturer report

Narratives

Additional Manufacturer Narrative · 1

THE BROKEN SUPPORT ARM HAS BEEN REQUESTED BACK FOR INVESTIGATION. A SUPPLEMENTAL MEDWATCH WILL BE PROVIDED AFTER INVESTIGATION. (B)(4).

Description of Event or Problem · 1

(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
225385 SUPPORT ARM 176 IOY MAQUET CRITICAL CARE AB

Patients

Seq Age Sex Outcome Treatment
1