HEA 1.2 BEADCHIP KIT, SLIDE 800-20202-08

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-09-21 for HEA 1.2 BEADCHIP KIT, SLIDE 800-20202-08 manufactured by Bioarray Solutions Ltd..

Event Text Entries

[121724430] Sequencing results interpretation: sequencing was unable to unequivocally differentiate the sample's allele identity at c. 676g>c; sequencing showed a definite major peak for cytosine as well as a background peak for guanine which would explain the e+ result1,2. Samples with similar background often have mixed chimerism from a hematopoetic stem cell transplantation or are contaminated; either could be the cause of the discrepancy between precisetype hea beadchip heag3656_8 and heag3662_1 phenotype results and serology results. The report was re-submitted to verify typo error on event description section. Lv 21sep2018. [(b)(4)].
Patient Sequence No: 1, Text Type: N, H10


[121724431] The customer reported a possible discrepancy. The donor is e+ using the bioarray hea molecular beadchip kit; serology results were e-.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005967741-2018-00015
MDR Report Key7899786
Date Received2018-09-21
Date of Report2018-09-21
Date of Event2018-08-22
Date Mfgr Received2018-08-22
Device Manufacturer Date2018-06-12
Date Added to Maude2018-09-21
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 ContactMS. LUZ VILLAMIZAR
Manufacturer Street35 TECHNOLOGY DRIVE SUITE 100
Manufacturer CityWARREN NJ 07059
Manufacturer CountryUS
Manufacturer Postal07059
Manufacturer Phone9084449591
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameHEA 1.2 BEADCHIP KIT, SLIDE
Generic NameHEA 1.2 BEADCHIP KIT, SLIDE
Product CodePEP
Date Received2018-09-21
Model Number800-20202-08
Catalog Number800-20202-08
Lot Number18-362
Device Expiration Date2019-05-31
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBIOARRAY SOLUTIONS LTD.
Manufacturer Address35 TECHNOLOGY DRIVE SUITE 100 WARREN NJ 07059 US 07059


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-21

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