LINDE INTEGRATED VALVE (LIV)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-12-31 for LINDE INTEGRATED VALVE (LIV) manufactured by .

Event Text Entries

[35246567] This is a spontaneous medical device incident report from (b)(6). On the (b)(6) 2015 a hospital worker handled a 2 liter aluminium cylinder with a new liv-valve from (b)(6) 2015 (from gce) containing conoxia (compressed medical oxygen) and an ignition occurred. The worker was not harmed. Pressure in the cylinder before the event was 10 mpa. A worker in the anesthesiology and resuscitation dept was holding the cylinder with medicinal oxygen in his hand. The cylinder was not connected to any other device nor pipeline. The worker should open the cylinder valve and set the regulated flow to 3. At this point, there was, according to his statement, in the first sparking phase and subsequent flame combustion. At the same time there was an abrupt pressure release and immediate emptying the contents of the pressure cylinder. Cylinder specification and identification liv - water capacity 2 litres - aluminium cylinder (gce). Cylinder id number: (b)(4). Cylinder icc barcode number: (b)(4). Filling pressure: 20mpa. Colour coding: white. Actual periodical pressure check: (b)(6) 2015. Integrated valve number: (b)(4). Cylinder filling date: (b)(6) 2015. Cylinder filling location: linde gas (b)(4). Distribution date: 11/19/2015. Distribution point: linde gas (b)(4). The fire-brigade have taken the cylinder and valve and these will be requested back to linde for further investigation. Additional information is expected. Pharmocovigilance comments: complaint report from health care provider in (b)(6) describing an accidental spontaneous ignition in an oxygen cylinder valve when the valve was opened. The ignition and fire was rapidly closed and no damage to property, and no patient nor personnel harm was observed. The valve is undergoing extensive internal and external investigation searching for root course. For reporting in accordance to regulations. (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5058984
MDR Report Key5350273
Date Received2015-12-31
Date of Report2015-12-31
Date of Event2015-12-04
Date Added to Maude2016-01-07
Event Key0
Report Source CodeVoluntary 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 Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLINDE INTEGRATED VALVE (LIV)
Generic NameLINDE INTEGRATED VALVE (LIV)
Product CodeECX
Date Received2015-12-31
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2015-12-31

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