FROVA INTUBATING INTRODUCER G48303 C-CAE-14.0-70-FIC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other,user facility report with the FDA on 2018-12-05 for FROVA INTUBATING INTRODUCER G48303 C-CAE-14.0-70-FIC manufactured by William Cook Europe.

Event Text Entries

[129297600] (b)(4). Name and address for importer site: (b)(4). Investigation is still in progress.
Patient Sequence No: 1, Text Type: N, H10


[129297601] Description of event according to initial reporter: "the product was used in a difficult intubation. After intubation they had fiberscopy to the patient, and they found 2 blue pieces of plastic in patient's airways. They were able to remove the other piece". Patient outcome: unknown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002808486-2018-01405
MDR Report Key8132379
Report SourceFOREIGN,OTHER,USER FACILITY
Date Received2018-12-05
Date of Report2019-02-22
Date of Event2018-11-12
Date Facility Aware2018-11-12
Date Mfgr Received2019-02-14
Device Manufacturer Date2018-10-02
Date Added to Maude2018-12-05
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 ContactMR. THOMAS HESSNER KIRK
Manufacturer StreetSANDET 6
Manufacturer CityBJAEVERSKOV DK-4632
Manufacturer CountryDA
Manufacturer PostalDK-4632
Manufacturer Phone56868686
Manufacturer G1WILLIAM COOK EUROPE
Manufacturer StreetSANDET 6
Manufacturer CityBJAEVERSKOV DK-4632
Manufacturer CountryDA
Manufacturer Postal CodeDK-4632
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFROVA INTUBATING INTRODUCER
Generic NameLRC INSTRUMENT, ENT MANUAL SURGICAL
Product CodeLRC
Date Received2018-12-05
Returned To Mfg2019-01-10
Model NumberG48303
Catalog NumberC-CAE-14.0-70-FIC
Lot NumberE3780483
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age1 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerWILLIAM COOK EUROPE
Manufacturer AddressSANDET 6 BJAEVERSKOV 4632 DA 4632


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-12-05

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