FLUID WARMING LEVEL 1 HOTLINE LOW FLOW SYSTEMS - HL-90 DOMESTIC HOTLINE 7803090

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other, report with the FDA on 2020-03-27 for FLUID WARMING LEVEL 1 HOTLINE LOW FLOW SYSTEMS - HL-90 DOMESTIC HOTLINE 7803090 manufactured by Smiths Medical Asd,inc.

Event Text Entries

[185479389] Information received a smith medical fluid warming
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02374
MDR Report Key9891607
Report SourceCOMPANY REPRESENTATIVE,OTHER,
Date Received2020-03-27
Date of Report2020-03-27
Date of Event2020-02-26
Date Mfgr Received2020-02-27
Date Added to Maude2020-03-27
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 ContactDAVE HALVERSON
Manufacturer Street6000 LANE N
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer Phone3833310
Manufacturer G1SMITHS MEDICAL ASD, INC.
Manufacturer Street3350 GRANADA AVENUE NORTH, SUITE 100
Manufacturer CityOAKDALE, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFLUID WARMING LEVEL 1 HOTLINE LOW FLOW SYSTEMS - HL-90
Generic NameWARMER, THERMAL, INFUSION FLUID
Product CodeLGZ
Date Received2020-03-27
Returned To Mfg2020-03-13
Model NumberDOMESTIC HOTLINE
Catalog Number7803090
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD,INC
Manufacturer Address6000 LANE N MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-27

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