FDA Adverse Event Malfunction Summary report: N

*

MDR report key: 45904 · Received October 25, 1996

Report

Report Number
45904
Event Type
Malfunction
Date Received
October 25, 1996
Date of Event
October 23, 1996
Report Date
October 25, 1996
Manufacturer
CONTINENTAL X-RAY CORP.
Product Code
KXJ
Product Problem
Yes
Report Source
User Facility report
Reporter Location
NJ, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

FLUOROSCOPY TABLE MALFUNCTIONED CAUSING PT TO SLIDE OFF FOOT END OF TABLE STRIKING HIS HEAD. PT ALSO SUSTAINED LACERATIONS. TREATED IN ER AND RELEASED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * RF TABLE KXJ CONTINENTAL X-RAY CORP. 6806.101 *

Patients

Seq Age Sex Outcome Treatment
1 57 YR DEVICE EVALUATED BY MFR, DAMAGED CHAIN TAKEN TO| FACTORY FOR ANALYSIS