LEVEL 1 HOTLINE LOW FLOW SYSTEMS HL-390 CON-HL-390

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-25 for LEVEL 1 HOTLINE LOW FLOW SYSTEMS HL-390 CON-HL-390 manufactured by Smiths Medical Asd, Inc.

Event Text Entries

[184996035] Evaluation results: one level 1 hotline low flow system was returned for investigation in used condition. There was damage to the main block. The tank was filled with water and a temp-check was attached to the unit. The unit was then powered on. The customer reported product problem was not confirmed during testing. Although the fluid flow was working fine, there was a leak at the plate clip however. The leak was attributed to a stripped interlock. The interlock was replaced as a result. A root cause was not established.
Patient Sequence No: 1, Text Type: N, H10


[184996036] It was reported that the fluid flow was not working on the device. No patient injury or complications were reported in relation to this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02288
MDR Report Key9880993
Report SourceUSER FACILITY
Date Received2020-03-25
Date of Report2020-03-25
Date Mfgr Received2020-02-27
Device Manufacturer Date2019-09-30
Date Added to Maude2020-03-25
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 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
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 NameLEVEL 1 HOTLINE LOW FLOW SYSTEMS
Generic NameWARMER, THERMAL, INFUSION FLUID
Product CodeLGZ
Date Received2020-03-25
Returned To Mfg2019-09-11
Model NumberHL-390
Catalog NumberCON-HL-390
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-25

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