FDA Adverse Event Other Summary report: N

CD3200 SL 110

MDR report key: 508685 · Received December 29, 2003

Report

Report Number
2919069-2003-00049
Event Type
Other
Date Received
December 29, 2003
Date of Event
November 20, 2003
Report Date
December 23, 2003
Manufacturer
ABBOTT LABORATORIES DIVISION/CELL DYN
Product Code
GKZ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
MEDICAL TECHNOLOGIST

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CD3200 SL 110 AUTOMATED HEMATOLOGY ANALYZER GKZ ABBOTT LABORATORIES DIVISION/CELL DYN NA NA

Patients

Seq Age Sex Outcome Treatment
1 81 YR Other