FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS BED

MDR report key: 3173471 · Received June 11, 2013

Report

Report Number
1824206-2013-03025
Event Type
Malfunction
Date Received
June 11, 2013
Date of Event
May 15, 2013
Report Date
May 15, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN TRIED TO REPAIR THIS BED THE FAMILY OF THE PATIENT WOULD NOT ALLOW THE TECHNICIAN TO REPAIR THE BED. NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THAT THE RIGHT SIDE RAIL WOULD NOT RISE. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
264163 TOTALCARE BARIATRIC PLUS BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1840

Patients

Seq Age Sex Outcome Treatment
1