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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NORTHGATE TECHNOLOGIES INC. In-Line Gas Warmer; CO2 GAS WARMING UNIT

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NORTHGATE TECHNOLOGIES INC. In-Line Gas Warmer; CO2 GAS WARMING UNIT Back to Search Results
Model Number 72-00204-0
Device Problem Thermal Decomposition of Device (1071)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 04/25/2019
Event Type  malfunction  
Manufacturer Narrative
The warmer, nti part number 72-00204-0; serial number: (b)(4) arrived at nti on 06/05/2019 from us distributor smith and nephew, inc.The unit was evaluated under nti capa (b)(4).The warmer was received disassembled and the cable was completely separated from the warmer cartridge.There was evidence of a high temperature event noted (e.G., the red wire insulation appeared to be melted away and fused to the blue wire).The warmer cartridge was then further dissected and a void was observed in the epoxy-filled cartridge cavity.Additionally, at the lemo connector, the collet nut was not seated all the way into the connector housing.This was caused by a mis-alignment of the connector body inside the connector shell.The mis-alignment was confirmed by a continuity check between the open wires and the pins on the connector.The connector body was found to be rotated one pin off center in the.Counterclockwise direction.A mis-alignment of the connector could result in an uncontrolled current going to the warmer (refer capa (b)(4)) causing overheating.The root cause of the overheating was most likely due to the mis-alignment of the lemo connector when the connector was reassembled.The separation of the cable from the warmer cartridge could be contributed by inadequate lap solder joints within the warmer cartridge.The mis-alignment issue of the lemo connector and inadequate solder joint issue have been addressed in capa (b)(4), respectively.All requests for additional information and clarification from the end user went unanswered.A device history record review (dhr) was conducted for the warmer under complaint (b)(4).The device history record for (b)(4) from september of 2017 (mo (b)(4)) was reviewed and the device passed all testing.Nothing out of the ordinary was noted.There have been no other complaints reported to nti for this device.Any additional findings will be updated via a follow-up report.
 
Event Description
On 05/30/2019, northgate technologies was made aware of an issue with an in-line warmer from distributor (b)(4) in the usa where it was alleged, "it was reported that the device started heating up and the cable started smoking, then the control unit turned off.No patient injury or significant delay were reported.Back up device was available.".
 
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Brand Name
In-Line Gas Warmer
Type of Device
CO2 GAS WARMING UNIT
Manufacturer (Section D)
NORTHGATE TECHNOLOGIES INC.
1591 scottsdale court
elgin IL 60123
Manufacturer (Section G)
NORTHGATE TECHNOLOGIES INC.
1591 scottsdale court
elgin IL 60123
Manufacturer Contact
todd gatto
1591 scottsdale court
elgin, IL 60123
2248562250
MDR Report Key8744812
MDR Text Key149671294
Report Number0001450997-2019-00003
Device Sequence Number1
Product Code HIF
UDI-Device Identifier03596010500601
UDI-Public03596010500601
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K972675
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 06/27/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/28/2019
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number72-00204-0
Device Catalogue Number7209944
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer06/05/2019
Date Manufacturer Received05/30/2019
Was Device Evaluated by Manufacturer? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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