FDA Adverse Event Other Summary report: N

CHLAMYDIAZYME EIA

MDR report key: 489423 · Received October 9, 2003

Report

Report Number
1415939-2003-00018
Event Type
Other
Date Received
October 9, 2003
Date of Event
September 10, 2003
Report Date
October 8, 2003
Manufacturer
ABBOTT LABORATORIES
Product Code
LJC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE ACCOUNT GENERATED NEGATIVE CHLAMYDIAZYME EIA RESULTS, REAGENT LOT 04572M100, ON 18 PTS THAT TESTED BSA SLIDE TECHNIQUE POSITIVE. THIS REPORT IS FOR PT 10 OF THE 18 TOTAL PTS. ALTHOUGH THE CONTROL VALUES WERE ACCEPTABLE, THE ACCOUNT NOTICED A BIG DROP IN THE POSITIVE RESULT VALUES AS COMPARED TO THE USUAL OBSERVED POSITIVE RESULT VALUES. THE ACCOUNT RETESTED THE PTS USING CHLAMYDIAZYME EIA REAGENT LOT 03228M100 WITH THE EXPECTED POSITIVE RESULTS. AMENDED REPORTS WERE SUBMITTED TO THE PHYSICIANS. IT IS UNKNOWN IF THERE WAS IMPACT TO PT MANAGEMENT. NO PT INFO IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CHLAMYDIAZYME EIA EIA FOR THE DETECTION OF CHLAMYDIA ANTIGEN LJC ABBOTT LABORATORIES NA 04572M100

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN QUANTUM II ANALYZER LIST 3303-13.