FDA Adverse Event Malfunction Summary report: N

POWER PRO TL

MDR report key: 2191866 · Received July 29, 2011

Report

Report Number
1831750-2011-07812
Event Type
Malfunction
Date Received
July 29, 2011
Date of Event
June 30, 2011
Report Date
July 1, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: STEERLOCK CROSS PIECE.

Description of Event or Problem · 1

IT WAS REPORTED THAT STEER LOCK WILL NOT DISENGAGE. THERE WAS NO REPORTED PT INVOLVEMENT OR ADVERSE CONSEQUENCES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 POWER PRO TL STRETCHER, WHEELED FPO STRYKER MEDICAL 6550 NA

Patients

Seq Age Sex Outcome Treatment
1