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OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM Adverse Event — Injury (MDR 1625425-2020-00304)

OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM Adverse Event — Injury (MDR 1625425-2020-00304) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM; Generic name: RETRIEVABLE IVC FILTER; Manufacturer: ARGON MEDICAL DEVICES.

DeviceOPTION RETRIEVABLE VENA CAVA FILTER SYSTEM
Generic nameRETRIEVABLE IVC FILTER
ManufacturerARGON MEDICAL DEVICES
Report number1625425-2020-00304
Event typeInjury
Product problemN
Date received2020-04-27
Report sourceSTUDY, USER FACILITY
NarrativeTHE SAMPLE DEVICE IS UNAVAILABLE FOR EVALUATION. WITHOUT SUCH EVIDENCE, THE COMPLAINT CANNOT BE CONFIRMED. IF ADDITIONAL INFORMATION IS PROVIDED IN THE FUTURE, THE ISSUE WILL BE RE-EVALUATED AS NEEDED.
SourceopenFDA MAUDE (device adverse events)

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