ARCHITECT TACROLIMUS 01L77-25

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-05-26 for ARCHITECT TACROLIMUS 01L77-25 manufactured by Abbott Laboratories.

Event Text Entries

[76191749] An evaluation is in process. A follow-up report will be submitted when the evaluation is complete. An evaluation is in-process.
Patient Sequence No: 1, Text Type: N, H10


[76191750] The customer observed one patient with a falsely elevated tacrolimus result while using the architect tacrolimus assay. The results were generated during treatment for a patient undergoing acute rejection for a heart transplant (received (b)(6) 2016). The customer indicated that 2 consecutive values which had been drawn on (b)(6) 2017 showed a falsely elevated, as follows: on (b)(6) 2017: 11. 2 mg/dl. On (b)(6) 2017: 44. 2 mg/dl. No impact to patient management was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1415939-2017-00118
MDR Report Key6594247
Report SourceHEALTH PROFESSIONAL
Date Received2017-05-26
Date of Report2017-07-20
Date of Event2017-05-03
Date Mfgr Received2017-06-20
Device Manufacturer Date2017-02-01
Date Added to Maude2017-05-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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 LABORATORIES
Manufacturer Street100 ABBOTT PARK ROAD
Manufacturer CityABBOTT PARK IL 600643500
Manufacturer CountryUS
Manufacturer Postal Code600643500
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARCHITECT TACROLIMUS
Generic NameTACROLIMUS
Product CodeMLM
Date Received2017-05-26
Catalog Number01L77-25
Lot Number72006M800
Device Expiration Date2018-06-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerABBOTT LABORATORIES
Manufacturer Address100 ABBOTT PARK ROAD ABBOTT PARK IL 600643500 US 600643500


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-26

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