BECTON DICKINSON 21261

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1997-06-26 for BECTON DICKINSON 21261 manufactured by Becton Dickinson Microbiology Systems.

Event Text Entries

[62064] Agar plates received are hemolized.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1011565
MDR Report Key101017
Date Received1997-06-26
Date of Report1997-06-25
Date Added to Maude1997-06-30
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationMEDICAL TECHNOLOGIST
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameBECTON DICKINSON
Generic NameBLOOD AGAR PLATES, BRUCELLA AGAR
Product CodeGSM
Date Received1997-06-26
Model NumberNA
Catalog Number21261
Lot NumberF4R4MM/E2NTJL
ID Number*
Device Expiration Date1997-08-12
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key99520
ManufacturerBECTON DICKINSON MICROBIOLOGY SYSTEMS
Manufacturer AddressPO BOX 243 COCKEYSVILLE MD 21030 US


Patients

Patient NumberTreatmentOutcomeDate
10 1997-06-26
20 1997-06-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.