ProductGuru Recalls

Official recall record

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Refer

US FDA — Medical Devices · 2024-07-19 · United StatesClass I
Issuing authority
US FDA — Medical Devices
Alert date
2024-07-19
Country of alert
United States
Alert level
Class I
Alert type
recall
Barcode (EAN/GTIN)
00850291007277
Brand on record
Inari Medical - Oak Canyon

What the authority reported

Thrombectomy system catheter instructions for use updated to reduce adverse events due to the following circumstances: 1) Fibrous, firmly adherent, calcified material, or suspected tumor thrombus overloading catheter bag 2) Catheter pulled through internal jugular vein access site or not pulled away from heart; may lead to device entrapment, pulmonary embolism, venous cutdown, abdominal surgery.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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