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 06 report with the FDA on 1997-05-07 for BACTEC MYCO/F-SPUTA CULTURE VIAL 4402187 manufactured by Becton Dickinson Microbiology Systems.

Event Text Entries

[59985] Customer reported that 6 to 7 bottles with cracked glass around seal of bottle. Some bottles leaked when placed into instrument. Pt specimens are negative to date for afb. No death or serious injury as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1119779-1997-00004
MDR Report Key89695
Report Source06
Date Received1997-05-07
Date of Report1997-04-30
Date of Event1997-04-18
Date Facility Aware1997-04-18
Report Date1997-04-30
Date Mfgr Received1997-04-18
Device Manufacturer Date1997-01-01
Date Added to Maude1997-05-13
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 Location3
Single Use3
Remedial ActionIN
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBACTEC MYCO/F-SPUTA CULTURE VIAL
Generic NameCULTURE MEDIA
Product CodeJSC
Date Received1997-05-07
Model NumberNA
Catalog Number4402187
Lot Number0157A
ID NumberNA
Device Expiration Date1998-02-01
OperatorOTHER
Device AvailabilityN
Device Age3 MO
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key88675
ManufacturerBECTON DICKINSON MICROBIOLOGY SYSTEMS
Manufacturer Address7 LOVETON CIRCLE SPARKS MD 211520999 US
Baseline Brand NameBACTEC MYCO/F-SPUTA CULTURE VIAL
Baseline Generic NameCULTURE MEDIA
Baseline Model NoNA
Baseline Catalog No4402187
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1997-05-07

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