FLOTEC DR813-700P4

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-03-22 for FLOTEC DR813-700P4 manufactured by Flotec.

Event Text Entries

[139586379] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[139586380] Day: (b)(6) 2019. Time: prior to 2:15 est. The user reported that some type of pop, flame, or ignition occurred as operator loosened dome handle on part # dr813-700p4, serial number (b)(4), before releasing pressure in the regulator. Unknown injury report. As of march 22, 2019 there has been no response to requests to a injury report.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1832475-2019-00003
MDR Report Key8444538
Report SourceCONSUMER
Date Received2019-03-22
Date Mfgr Received2019-03-04
Device Manufacturer Date2009-07-10
Date Added to Maude2019-03-22
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 ContactJOHN PICHON
Manufacturer Street7625 WEST NEW YORK STREET
Manufacturer CityINDIANAPOLIS IN 46214
Manufacturer CountryUS
Manufacturer Postal46214
Manufacturer Phone3172736960
Manufacturer G1FLOTEC
Manufacturer Street7625 WEST NEW YORK STREET
Manufacturer CityINDIANAPOLIS IN 46214
Manufacturer CountryUS
Manufacturer Postal Code46214
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFLOTEC
Generic NameINGAGE REGULATOR
Product CodeCAN
Date Received2019-03-22
Model NumberDR813-700P4
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerFLOTEC
Manufacturer Address7625 WEST NEW YORK STREET INDIANAPOLIS IN 46214 US 46214


Patients

Patient NumberTreatmentOutcomeDate
10 2019-03-22

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