ACCESS VITAMIN B12 REAGENT 33000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-11-15 for ACCESS VITAMIN B12 REAGENT 33000 manufactured by Beckman Coulter.

MAUDE Entry Details

Report Number2122870-2019-01140
MDR Report Key9329281
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2019-11-15
Date of Report2019-11-15
Date of Event2019-10-30
Date Facility Aware2019-11-01
Date Mfgr Received2019-11-01
Device Manufacturer Date2019-06-01
Date Added to Maude2019-11-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. DAVID DAVIS
Manufacturer Street250 S. KRAEMAR BLVD.
Manufacturer CityBREA CA 928218000
Manufacturer CountryUS
Manufacturer Postal928218000
Manufacturer Phone7149613796
Manufacturer G1BECKMAN COULTER
Manufacturer Street1000 LAKE HAZELTINE DRIVE
Manufacturer CityCHASKA MN 55318
Manufacturer CountryUS
Manufacturer Postal Code55318
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACCESS VITAMIN B12 REAGENT
Generic NameRADIOASSAY, VITAMIN B12
Product CodeCDD
Date Received2019-11-15
Model Number33000
Catalog Number33000
Lot Number921022
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER
Manufacturer Address1000 LAKE HAZELTINE DRIVE CHASKA MN 55318 US 55318


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-15

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