FDA Adverse Event Malfunction Summary report: N

LABOR & DELIVERY BED

MDR report key: 1874977 · Received October 13, 2010

Report

Report Number
1831750-2010-02832
Event Type
Malfunction
Date Received
October 13, 2010
Date of Event
September 16, 2010
Report Date
September 16, 2010
Manufacturer
STRYKER CORP. MEDICAL DIV.
Product Code
HDD
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: TREND ACTUATOR ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE TREND IS NOT WORKING. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LABOR & DELIVERY BED LABOR AND DELIVERY BED HDD STRYKER CORP. MEDICAL DIV. 5010 NA

Patients

Seq Age Sex Outcome Treatment
1