BACT/ALERT SN CULTURE BOTTLE 259790

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2008-08-27 for BACT/ALERT SN CULTURE BOTTLE 259790 manufactured by Biomerieux, Inc..

Event Text Entries

[930746] While unloading a bact/alert sn blood culture bottle from the incubator, the cap and rubber stopper came off of a bottle which was positive with a positive with a (b) (6). The sample splashed onto the user's laboratory coat and into the cells below and drip pan.
Patient Sequence No: 1, Text Type: D, B5


[8197901] An investigation of the event has been initiated. Additional information will be provided when it becomes available.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3002769706-2008-00006
MDR Report Key1139002
Report Source06
Date Received2008-08-27
Date of Report2008-08-29
Date of Event2008-07-31
Date Mfgr Received2008-07-31
Device Manufacturer Date2008-03-01
Date Added to Maude2010-04-14
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 ContactELIZABETH FRITZ
Manufacturer Street100 RODOLPHE ST
Manufacturer CityDURHAM NC 27712
Manufacturer CountryUS
Manufacturer Postal27712
Manufacturer Phone9196202682
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBACT/ALERT SN CULTURE BOTTLE
Generic NameMICROBIAL GROWTH MONITOR
Product CodeJTA
Date Received2008-08-27
Catalog Number259790
Lot Number1020021
Device Expiration Date2009-03-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX, INC.
Manufacturer Address100 RODOLPHE ST DURHAM NC US


Patients

Patient NumberTreatmentOutcomeDate
10 2008-08-27

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