FDA Adverse Event Malfunction Summary report: N

MANUAL BED

MDR report key: 1677735 · Received April 27, 2010

Report

Report Number
1824206-2010-06456
Event Type
Malfunction
Date Received
April 27, 2010
Date of Event
March 31, 2010
Report Date
March 31, 2010
Manufacturer
HILL-ROM RITTER
Product Code
FNJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT REPLACED THE LEFT FOOT BRAKE CASTER TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES, THE LEFT FOOT BRAKE WILL NOT HOLD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MANUAL BED MANUAL BED FNJ HILL-ROM RITTER 426

Patients

Seq Age Sex Outcome Treatment
1