FDA Adverse Event Malfunction Summary report: N

HMX-5 MOBILE X-RAY UNIT

MDR report key: 271171 · Received March 23, 2000

Report

Report Number
1220984-2000-00005
Event Type
Malfunction
Date Received
March 23, 2000
Date of Event
February 1, 2000
Report Date
March 23, 2000
Manufacturer
TREX MEDICAL SYSTEMS CORP.
Product Code
IZL
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE RIGHT FRONT CASTER BROKE WHILE MOVING THE MACHINE. ACCORDING TO THE REPORT, THE OPERATOR'S WRIST WAS BROKEN AS A RESULT OF THE INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HMX-5 MOBILE X-RAY UNIT RADIOLOGIC IZL TREX MEDICAL SYSTEMS CORP. HMX-5 NA

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN