FDA Adverse Event Malfunction Summary report: N

CAREASSIST BED CA30

MDR report key: 3874465 · Received December 27, 2012

Report

Report Number
3006697241-2012-00318
Event Type
Malfunction
Date Received
December 27, 2012
Manufacturer
HILLROM DE MEXICO S DE RL DE CV
Product Code
FNL
Report Source
Manufacturer report

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ISOLATED THE ISSUE TO A STUCK HEAD UP BUTTON ON THE PENDANT, CAUSING THE HEAD SECTION TO RISE ON ITS OWN. THE TECHNICIAN REPLACED THE PENDANT TO REPAIR THE BED.

Description of Event or Problem · 1

PLEASE REFER IMPORTER REPORT # (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAREASSIST BED CA30 AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILLROM DE MEXICO S DE RL DE CV

Patients

Seq Age Sex Outcome Treatment
1