AXP AUTOXPRESS PLATFORM 8-5101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2008-11-17 for AXP AUTOXPRESS PLATFORM 8-5101 manufactured by Thermogenesis Corp..

Event Text Entries

[989316] A customer called to report that white debris was found in the freezing bag.
Patient Sequence No: 1, Text Type: D, B5


[8233172] This lot is included in a recall notification sent to fda in 2008. An assigned fda recall number is still pending at the time of writing. Internally, we have identified this recall. No adverse event has been reported for this occurence.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2950374-2008-00002
MDR Report Key1239127
Report Source04
Date Received2008-11-17
Date of Report2008-11-17
Date of Event2008-10-27
Date Mfgr Received2008-10-27
Device Manufacturer Date2008-02-01
Date Added to Maude2009-06-05
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 FDA0
Event Location0
Manufacturer ContactTRISTA MADSEN
Manufacturer Street2711 CITRUS RD.
Manufacturer CityRANCHO CORDOVA CA 95742
Manufacturer CountryUS
Manufacturer Postal95742
Manufacturer Phone9168585109
Single Use3
Remedial ActionRC
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAXP AUTOXPRESS PLATFORM
Product CodeOAO
Date Received2008-11-17
Model Number8-5101
Catalog Number8-5101
Lot Number08B25
ID NumberNA
Device Expiration Date2009-01-31
OperatorHEALTH PROFESSIONAL
Device AgeNA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTHERMOGENESIS CORP.
Manufacturer Address2711 CITRUS RD. RANCHO CORDOVA CA 95742 US 95742


Patients

Patient NumberTreatmentOutcomeDate
10 2008-11-17

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