FDA Adverse Event Other Summary report: N

DAC II

MDR report key: 14860 · Received July 25, 1994

Report

Report Number
MW1002927
Event Type
Other
Date Received
July 25, 1994
Date of Event
July 9, 1994
Report Date
July 14, 1994
Manufacturer
DADE DIV. BAXTER HEALTHCARE CORP.
Product Code
KSN
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
MEDICAL TECHNOLOGIST

Narratives

Description of Event or Problem · 1

EQUIPMENT WORKED WELL AT BEGINNING OF SHIFT. AROUND 10 AM IT WOULD NOT START CYCLE SO IT WAS RESET BY TURNING OFF AND ON. WHEN IT WAS USED A SHORT TIME LATER IT WOULD NOT START AGAIN SO IT WAS UNPLUGGED FOR A BRIEF TIME. WHEN IT STILL WOULD NOT START THE FUSES WERE CHECKED. IT WAS TURNED OFF AND ON SEVERAL MORE TIMES BUT WOULD NOT START. IT WAS LEFT PLUGGED IN WITH THE LID CLOSED. ABOUT 11:30 RPTR SMELLED SMOKE AND SAW THAT IT WAS COMING FROM THE CELL WASHER. UNPLUGGED EQUIPMENT AND CALLED FOR FIRE CREW.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DAC II AUTOMATIC TUBE WASHER KSN DADE DIV. BAXTER HEALTHCARE CORP. DAC2

Patients

Seq Age Sex Outcome Treatment
1 * Other