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INARI MEDICAL Recalls
1 recall on record · June 17, 2020 to June 17, 2020 · Medical Devices
June 17, 2020
Medical Devices
FDA
INARI MEDICAL recalls Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Hazard: The hemostasis valve of aspiration guide catheter devices may fail to seal resulting in a loss of vacuum during thrombus aspiration, which may result the procedure being prolonged as another device must be used or suboptimal thrombus removal if the problem is not detected.
INARI MEDICAL Recalls | RecallWatchUSA