ARCHITECT IVANCOMYCIN 01P30-27

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-09-17 for ARCHITECT IVANCOMYCIN 01P30-27 manufactured by Abbott Germany.

Event Text Entries

[120839814] An evaluation is in process. A follow-up report will be submitted when the evaluation is complete. This report is being filed on an international product, list number 1p30-27 that has a similar product distributed in the us, list number 1p30-28. An evaluation is in process.
Patient Sequence No: 1, Text Type: N, H10


[120839815] The customer observed falsely depressed results while using architect ivancomycin reagents. The following data was provided. Sid (b)(6) initial (tested 9:25 a. M. ) 0. 24 ug/ml, repeat (tested 10:00 a. M. ) 64. 78 ug/ml. No impact to patient management was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002809144-2018-00345
MDR Report Key7882946
Date Received2018-09-17
Date of Report2018-10-26
Date of Event2018-08-27
Date Mfgr Received2018-10-10
Device Manufacturer Date2018-02-01
Date Added to Maude2018-09-17
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 GERMANY
Manufacturer StreetMAX-PLANCK-RING 2
Manufacturer CityWIESBADEN 65205
Manufacturer CountryGM
Manufacturer Postal Code65205
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameARCHITECT IVANCOMYCIN
Generic NameVANCOMYCIN
Product CodeLEH
Date Received2018-09-17
Catalog Number01P30-27
Lot Number00118A000
Device Expiration Date2019-06-21
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerABBOTT GERMANY
Manufacturer AddressMAX-PLANCK-RING 2 WIESBADEN 65205 GM 65205


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-17

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