MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1997-07-02 for BACTEC MYCO/F-SPUTA CULTURE VIAL 4402187 manufactured by Becton Dickinson Microbiology Systems.
[57696]
Customer reported leaking of one vial after inoculation of specimen. Customer reported that specimen was positive for mycobacteria. No death or serious injury has occurred as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1119779-1997-00009 |
MDR Report Key | 102661 |
Report Source | 05 |
Date Received | 1997-07-02 |
Date of Report | 1997-06-09 |
Date of Event | 1997-06-09 |
Date Mfgr Received | 1997-06-09 |
Device Manufacturer Date | 1997-01-01 |
Date Added to Maude | 1997-07-07 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Single Use | 3 |
Remedial Action | IN |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BACTEC MYCO/F-SPUTA CULTURE VIAL |
Generic Name | CULTURE MEDIA |
Product Code | JSC |
Date Received | 1997-07-02 |
Model Number | NA |
Catalog Number | 4402187 |
Lot Number | 0157A |
ID Number | NA |
Device Expiration Date | 1998-02-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 101032 |
Manufacturer | BECTON DICKINSON MICROBIOLOGY SYSTEMS |
Manufacturer Address | 7 LOVETON CIRCLE SPARKS MD 21152 US |
Baseline Brand Name | BACTEC MYCO/F-SPUTA CULTURE VIAL |
Baseline Generic Name | CULTURE MEDIA |
Baseline Model No | NA |
Baseline Catalog No | 4402187 |
Baseline ID | NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1997-07-02 | |
2 | 0 | 1997-07-02 |