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CT Thrombectomy System Kit

Inari Medical, Inc. · Model 90-101 · UDI-DI 00850291007154

DXE Prescription
10
510(k) clearances
7,736
Adverse events (143 deaths)
57
Recalls
41
Facilities

Description

CT Thrombectomy System Kit - Contains x1 ClotTriever Catheter (40-102) and x1 ClotTriever Sheath (50-101)

Recalls

DateFirmReason
2026-04-21PFM MEDICAL INC.A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-
2025-04-11LeMaitre Vascular, Inc.During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
2024-04-17LeMaitre Vascular, Inc.The guide tip can become damaged and result in the tip detaching.
2023-09-07Edwards Lifesciences, LLCInadvertent release of embolectomy catheters that may experience slower than normal balloon deflation (greater-than 15 seconds).
2022-10-06Edwards Lifesciences, LLCDue to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches.
2022-10-06Edwards Lifesciences, LLCDue to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches.
2022-09-30LeMaitre Vascular, Inc.Three lots tied by two trainees were released without performing the required pull test. If tied with inadequate strength, the proximal ligature could slip toward the tip of the ca
2021-09-20Arrow International Inc7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached from the device basket result in embolization and retrieval with an additional intervention and consequent
2021-09-20Arrow International Inc7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached from the device basket result in embolization and retrieval with an additional intervention and consequent
2021-09-20Arrow International Inc7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached from the device basket result in embolization and retrieval with an additional intervention and consequent

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.