BACTEC MYCO/F-SPUTA CULTURE VIAL 4402187

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1998-03-16 for BACTEC MYCO/F-SPUTA CULTURE VIAL 4402187 manufactured by Becton Dickinson Microbiology Systems.

Event Text Entries

[19159841] Customer reported leaking of 1 vial after inoculation of specimen. Customer reported that initial smear results were negative. The solid media grew and identified as mac. No death or serious injury has occurred as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1119779-1998-00002
MDR Report Key157529
Report Source05
Date Received1998-03-16
Date of Report1998-02-13
Date of Event1998-02-13
Date Mfgr Received1998-02-13
Device Manufacturer Date1997-05-01
Date Added to Maude1998-03-20
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBACTEC MYCO/F-SPUTA CULTURE VIAL
Generic NameCULTURE MEDIA
Product CodeJSI
Date Received1998-03-16
Model NumberNA
Catalog Number4402187
Lot Number0057E
ID NumberNA
Device Expiration Date1998-06-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key153475
ManufacturerBECTON DICKINSON MICROBIOLOGY SYSTEMS
Manufacturer Address7 LOVETON CIRCLE SPARKS MD 21152 US
Baseline Brand NameBACTEC MYCO/F-SPUTA CULTURE VIAL
Baseline Generic NameCULTURE MEDIA
Baseline Model NoNA
Baseline Catalog No4402187
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 1998-03-16

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