FDA Adverse Event Malfunction Summary report: N

REMB SAG SAW

MDR report key: 2231266 · Received July 25, 2011

Report

Report Number
1811755-2011-02665
Event Type
Malfunction
Date Received
July 25, 2011
Date of Event
June 28, 2011
Report Date
June 28, 2011
Manufacturer
STRYKER INSTRUMENTS KALAMAZOO
Product Code
HBE
PMA / PMN Number
K032303
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE REMB SAG SAW WAS SENT IN FOR SERVICE AND IT OVERHEATED DURING PERFORMANCE TESTING. NO ADVERSE EVENT WAS ASSOCIATED WITH THE DEVICE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 REMB SAG SAW HBE STRYKER INSTRUMENTS KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1 UNK