LIV LIV 2000 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-06-15 for LIV LIV 2000 * manufactured by Linde Gas North America Llc.

Event Text Entries

[6834882] Oxygen tank on crash cart malfunctioned for use with code blue. Gauge on o2 tank read "full" valve was "open" and the oxygen dial for selecting liters/min was fully turned up to the max (15l/m). However, no oxygen flowed from regulator of tank. Multiple attempts were made to reopen and close valve and liters/min to try to open the oxygen tank with no success.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number4901766
MDR Report Key4901766
Date Received2015-06-15
Date of Report2015-06-10
Date of Event2015-06-04
Report Date2015-06-10
Date Reported to FDA2015-06-15
Date Reported to Mfgr2015-07-09
Date Added to Maude2015-07-09
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameLIV
Generic NameCYLINDER, COMPRESSED GAS, AND VALVE
Product CodeECX
Date Received2015-06-15
Returned To Mfg2015-06-08
Model NumberLIV 2000
Catalog Number*
Lot Number201209 35
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age*
Device Sequence No1
Device Event Key0
ManufacturerLINDE GAS NORTH AMERICA LLC
Manufacturer Address575 MOUNTAIN AVE. MURRAY HILL NJ 07974 US 07974


Patients

Patient NumberTreatmentOutcomeDate
10 2015-06-15

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