Inari Medical recalls Triever20 Aspiration Guide Catheters with UDI 00850291007079 due to potential vacuum loss during thrombus aspiration, risking prolonged procedures or incomplete clot removal.
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 is recalling Triever20 Aspiration Guide Catheters that could lose vacuum during thrombus removal, potentially requiring additional devices or incomplete clot removal. This affects medical procedures where precise clot extraction is critical.
The hemostasis valve in the catheter may fail to seal properly, causing vacuum loss during clot removal. This could require switching to another device or lead to suboptimal clot extraction if not detected.
Healthcare professionals using the Triever20 Aspiration Guide Catheter in thrombus aspiration procedures are most at risk. Patients undergoing these procedures may experience prolonged treatment or incomplete clot removal.
Check for the UDI code 00850291007079 on the catheter. The affected lot numbers are 20010004, 20010005, and 20010008.
Verify the UDI code and lot numbers on the catheter to confirm if it is affected.
The hemostasis valve may fail to seal, causing vacuum loss during thrombus aspiration, which could prolong procedures or lead to incomplete clot removal.
Check the UDI code and lot numbers to confirm if it is affected. If affected, contact Inari Medical for further instructions.
Yes, patients may experience prolonged procedures or incomplete clot removal if the catheter fails to seal properly.
We’ve drafted a message you can send Inari Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2299-2020 — Inari Medical Inari Medical Hello, I own a Inari Medical that is covered by recall Z-2299-2020 from Inari Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
