FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 3172402 · Received June 17, 2013

Report

Report Number
0001831750-2013-05462
Event Type
Malfunction
Date Received
June 17, 2013
Date of Event
May 21, 2013
Report Date
May 21, 2013
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE BASE WILL NOT RETRACT IN POWERED OR MANUAL MODE. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
272816 POWER PRO AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1