FDA Adverse Event Malfunction Summary report: N

HILL-ROM 1000 BED

MDR report key: 2113322 · Received May 25, 2011

Report

Report Number
3006697241-2011-00043
Event Type
Malfunction
Date Received
May 25, 2011
Date of Event
May 4, 2011
Report Date
May 4, 2011
Manufacturer
HILL-ROM DE MEXICO S DE RL DE CV
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REPAIRS HAVE NOT BEEN COMPLETED.

Description of Event or Problem · 1

INFO REC'D INDICATES THE HI/LOW COLUMN CAME OUT OF ITS SUPPORT WHICH CAUSED THE HI/LOW COLUMN TO COME IN CONTACT WITH THE HEAD SECTION FRAME WHICH BENT THE HEAD SECTION FRAME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HILL-ROM 1000 BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM DE MEXICO S DE RL DE CV 1160

Patients

Seq Age Sex Outcome Treatment
1 UNK