FDA Adverse Event Malfunction Summary report: N

TOTAL CARE BED

MDR report key: 2053485 · Received March 17, 2011

Report

Report Number
1824206-2011-01641
Event Type
Malfunction
Date Received
March 17, 2011
Date of Event
November 30, 2009
Report Date
November 30, 2009
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DA
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE POWER CORD TO RESOLVE THE ISSUE. THIS MDR IS A RESULT OF CAPA ACTIVITY FOR THE RETROSPECTIVE REVIEW OF COMPLAINTS.

Description of Event or Problem · 1

ACCOUNT ALLEGED THAT THE BED HAD NO FUNCTION. NO PATIENT IMPACT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1