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UNKNOWN Adverse Event — Injury (MDR 3002808486-2020-00452)

UNKNOWN Adverse Event — Injury (MDR 3002808486-2020-00452) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN; Generic name: DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR; Manufacturer: WILLIAM COOK EUROPE.

DeviceUNKNOWN
Generic nameDTK FILTER, INTRAVASCULAR, CARDIOVASCULAR
ManufacturerWILLIAM COOK EUROPE
Report number3002808486-2020-00452
Event typeInjury
Product problemN
Date received2020-04-27
Report sourceCONSUMER
NarrativeADDITIONAL INFORMATION PROVIDED DETERMINED THAT THIS DEVICE WAS MANUFACTURED BY COOK INC. WITH THE SUBMISSION OF THIS FOLLOW UP REPORT, WILLIAM COOK EUROPE INFORMS THAT THIS COMPLAINT HAS BEEN TRANSFERRED FROM WILLIAM COOK EUROPE TO COOK INC. THIS REPORT IS REQUIRED BY THE FDA UNDER 21 CFR PART 803 AND IS BASED ON UNCONFIRMED INFORMATION SUBMITTED BY OTHERS. NEITHER THE SUBMISSION OF THIS REPORT N
SourceopenFDA MAUDE (device adverse events)

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