Reported Jun 17, 2020 · Terminated
Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Inari Medical
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: INARI MEDICAL · 9 Parker Ste 100 · Irvine, CA · 92618-1666
Is this the product you have?
- Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System
- UDI00850291007079
- Lot codes and dates
- Lot
200100042001000520010008
- Lot
- Amount recalled
- 318
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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