ARCHITECT CEA 07K68-35

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 2019-01-30 for ARCHITECT CEA 07K68-35 manufactured by Abbott Ireland.

Event Text Entries

[134503152] An evaluation is in process. A follow up report will be submitted when the evaluation is complete. (b)(4). No adverse impact was reported due to the procedures.
Patient Sequence No: 1, Text Type: N, H10


[134503153] The customer reported a false elevated architect cea result. The sample generated a result of 50. 3 ng/ml. The patient's previous result was 28. 1 ng/ml. The customer indicated the patient had a pet-ct, colon fiberscope and gastroscopy due to the elevated cea results. There was no adverse impact to the patient due to the procedures.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008344661-2019-00007
MDR Report Key8289790
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2019-01-30
Date of Report2019-07-03
Date Mfgr Received2019-06-18
Device Manufacturer Date2018-09-04
Date Added to Maude2019-01-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
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 Received2019-01-30
Catalog Number07K68-35
Lot Number90351FN00
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
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
101. Deathisabilit 2019-01-30

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