FDA Adverse Event Malfunction Summary report: N

SECURE 3 MED/SURG BED

MDR report key: 2142814 · Received June 20, 2011

Report

Report Number
1831750-2011-06183
Event Type
Malfunction
Date Received
June 20, 2011
Date of Event
May 23, 2011
Report Date
May 23, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

CONCLUSION: REPLACEMENT NURSE CALL CABLE HAS BEEN ORDERED AND THE CUSTOMER WILL INSTALL IT WHEN IT IS RECEIVED.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE NURSE CALL WILL NOT WORK ON THE BED. THE CABLE WAS DISCONNECTED AND FRAYED. THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002S3EX NA

Patients

Seq Age Sex Outcome Treatment
1