THROMBOTYPE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other,study report with the FDA on 2018-06-29 for THROMBOTYPE manufactured by Immucor Gti Diagnostics, Inc..

Event Text Entries

[113189644] Thrombotype lot 3005154 (expiration date 08-15-2018) failed to meet testing specifications during 15-month stability testing due to weak and/or absent bands in the hpa-1a and hpa-3a systems during the initial testing on 05/30/2018. The failure mode observed in oos 18-98 was confirmed during repeat testing. Oos 18-98 was initiated to investigate weak and/or absent bands in the hpa-1a and hpa-3a systems during repeat testing on (b)(6) 2018. Alternate samples were tested under oos 18-98, to rule out sample integrity. The replacement samples showed weak/absent bands for hpa-1a and absent bands for hpa-3a. The failures were isolated to the hpa-1a and hpa-3a systems indicating that the other test kit components are performing as expected. This indicates potential degradation of the hpa-1a and hpa-3a primers. A review of similar products in the field identified thrombotype 1 lots 3006502 and 3005160. Thrombotype 1 lot 3005160 was manufactured with the same lots of primer raw materials for the hpa-1a system. The 18 month stability time point was completed on 06/19/2018 and all specifications were met. Therefore, this failure appears to be specific to the manufacture of the thrombotype lot 3005154 primer tubes (primer tube lot 300570). Thrombotype 1 lot 3006502 was manufactured with different lots of primer raw materials for the hpa-1a system. At this time, the root cause is considered to be degradation of the hpa-1a and hpa-3a primers specific to the manufacture of thrombotype primer tube lot 3005070. A review of the thrombotype primer tube lot 3005070 manufacturing records was performed; a specific root cause for the observed failures could not be identified. Further investigation testing into the failure is not able to be performed due to unavailability of adequate kits from thrombotype lot 3005154. Thrombotype lot 3005154 is the only lot of thrombotype currently in the market.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2183608-2018-00026
MDR Report Key7652289
Report SourceOTHER,STUDY
Date Received2018-06-29
Date of Report2018-06-13
Date of Event2018-06-11
Device Manufacturer Date2017-03-21
Date Added to Maude2018-06-29
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 JOAN RIXE
Manufacturer Street20925 CROSSROADS CIRCLE
Manufacturer CityWAUKESHA WI 53186
Manufacturer CountryUS
Manufacturer Postal53186
Manufacturer Phone2627541016
Manufacturer G1IMMUCOR GTI DIAGNOSTICS, INC.
Manufacturer Street20925 CROSSROADS CIRCLE
Manufacturer CityWAUKESHA WI 53186
Manufacturer CountryUS
Manufacturer Postal Code53186
Single Use3
Remedial ActionNO
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHROMBOTYPE
Generic NameTHROMBOTYPE
Product CodeMYP
Date Received2018-06-29
Catalog NumberTHROMBOTYPE
Lot Number3005154
Device Expiration Date2018-08-15
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerIMMUCOR GTI DIAGNOSTICS, INC.
Manufacturer Address20925 CROSSROADS CIRCLE WAUKESHA WI 53186 US 53186


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-29

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