FDA Adverse Event Malfunction Summary report: N

DIAGNOST 66

MDR report key: 12043 · Received March 15, 1994

Report

Report Number
MW1001089
Event Type
Malfunction
Date Received
March 15, 1994
Date of Event
February 17, 1994
Report Date
March 3, 1994
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
KXJ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
VA, US
Reporter Occupation
RADIOLOGIC TECHNOLOGIST

Narratives

Description of Event or Problem · 1

PT WAS HAVING UPPER GI X-RAYS TAKEN. TABLE WAS HORIZONTAL. PT WAS TURNING AND HOLDING ON TO UPPER EDGE OF TABLE. HAND BAR WAS IN PLACE. PT HAD BEEN INSTRUCTED BY TECHNOLOGIST TO HOLD ONTO HAND BAR. PT THOUGHT SHE WAS HOLDING HAND BAR BUT ACTUALLY WAS HOLDING ON TO THE TOP EDGE OF THE TABLE. RADIOLOGIST MOVED THE TABLE TOP AND THE 2 FINGERS ON HER RIGHT HAND WERE CAUGHT IN EDGE OF TABLE. FINGERS WERE LACERATED AND PART OF ONE NAIL REMOVED. REQUIRED SPLINTING OF FINGERS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DIAGNOST 66 KXJ PHILIPS MEDICAL SYSTEMS

Patients

Seq Age Sex Outcome Treatment
1 25 YR Other