CADD CASSETTE RESERVOIR 21-7302-24

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other,use report with the FDA on 2019-11-14 for CADD CASSETTE RESERVOIR 21-7302-24 manufactured by Smiths Medical Asd,inc.

MAUDE Entry Details

Report Number3012307300-2019-06473
MDR Report Key9325293
Report SourceHEALTH PROFESSIONAL,OTHER,USE
Date Received2019-11-14
Date of Report2019-11-14
Date of Event2019-10-15
Date Mfgr Received2019-10-15
Date Added to Maude2019-11-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactDAVE HALVERSON
Manufacturer Street6000 LANE N
Manufacturer CityMINNEAPOLIS MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone7633833310
Manufacturer G1SMITHS MEDICAL ASD,INC
Manufacturer Street6000 LANE N
Manufacturer CityMINNEAPOLIS MN 55442
Manufacturer CountryUS
Manufacturer Postal Code55442
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCADD CASSETTE RESERVOIR
Generic NameACCESSORIES, PUMP, INFUSION
Product CodeMRZ
Date Received2019-11-14
Returned To Mfg2019-10-18
Catalog Number21-7302-24
Lot Number3776385
Device Expiration Date2019-03-13
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD,INC
Manufacturer Address6000 LANE N MINNEAPOLIS MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-14

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