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..
[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
Report Number | 3005967741-2018-00015 |
MDR Report Key | 7899786 |
Date Received | 2018-09-21 |
Date of Report | 2018-09-21 |
Date of Event | 2018-08-22 |
Date Mfgr Received | 2018-08-22 |
Device Manufacturer Date | 2018-06-12 |
Date Added to Maude | 2018-09-21 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. LUZ VILLAMIZAR |
Manufacturer Street | 35 TECHNOLOGY DRIVE SUITE 100 |
Manufacturer City | WARREN NJ 07059 |
Manufacturer Country | US |
Manufacturer Postal | 07059 |
Manufacturer Phone | 9084449591 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | HEA 1.2 BEADCHIP KIT, SLIDE |
Generic Name | HEA 1.2 BEADCHIP KIT, SLIDE |
Product Code | PEP |
Date Received | 2018-09-21 |
Model Number | 800-20202-08 |
Catalog Number | 800-20202-08 |
Lot Number | 18-362 |
Device Expiration Date | 2019-05-31 |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOARRAY SOLUTIONS LTD. |
Manufacturer Address | 35 TECHNOLOGY DRIVE SUITE 100 WARREN NJ 07059 US 07059 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-09-21 |