FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2063863 · Received April 12, 2011

Report

Report Number
1824206-2011-02121
Event Type
Malfunction
Date Received
April 12, 2011
Date of Event
March 19, 2011
Report Date
March 19, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE CAUSE TO BE A STUCK HEAD UP VALVE TO THE HEAD SECTION. THE TECHNICIAN REPLACED THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

ACCOUNT ALLEGED THAT THE HEAD OF THE BED WILL NOT RAISE. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1