FDA Adverse Event Malfunction Summary report: N

IN TOUCH ZX

MDR report key: 2231213 · Received July 18, 2011

Report

Report Number
1831750-2011-07153
Event Type
Malfunction
Date Received
July 18, 2011
Date of Event
June 20, 2011
Report Date
June 20, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

SIDERAIL DAMAGE.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT SIDE RAIL WOULD NOT LOCK IN THE UP POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IN TOUCH ZX A/C HOSPITAL BED FNL STRYKER MEDICAL 2140 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK