ARCHITECT CEA 07K68-25

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2018-12-04 for ARCHITECT CEA 07K68-25 manufactured by Abbott Ireland.

Event Text Entries

[130178235] An evaluation is in process. A follow-up report will be submitted when the evaluation is complete.
Patient Sequence No: 1, Text Type: N, H10


[130178236] The customer observed falsely depressed results while using architect cea (carcinoembryonic antigen) reagents. The following data was provided for the same patient. Tested (b)(6) 2018 5. 9 ng/ml. Previous and subsequent results were higher when tested on (b)(6) 2018 (302. 5 ng/ml) and (b)(6) 2018 (430. 8 ng/ml). No impact to patient management was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008344661-2018-00101
MDR Report Key8131062
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2018-12-04
Date of Report2019-01-23
Date of Event2018-10-19
Date Mfgr Received2019-01-11
Date Added to Maude2018-12-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactNOEMI ROMERO-KONDOS, RN BSN
Manufacturer Street100 ABBOTT PARK ROAD DEPT. 09B9, LCCP1-3
Manufacturer CityABBOTT PARK IL 600643537
Manufacturer CountryUS
Manufacturer Postal600643537
Manufacturer Phone224667-512
Manufacturer G1ABBOTT IRELAND
Manufacturer StreetDIAGNOSTICS DIVISION FINISKLIN BUSINESS PARK
Manufacturer CitySLIGO NA
Manufacturer CountryEI
Manufacturer Postal CodeNA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARCHITECT CEA
Generic NameCARCINOEMBRYONIC ANTIGEN
Product CodeDHX
Date Received2018-12-04
Catalog Number07K68-25
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerABBOTT IRELAND
Manufacturer AddressDIAGNOSTICS DIVISION FINISKLIN BUSINESS PARK SLIGO NA EI NA


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-04

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.