FDAJuly 19, 2024device

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

FDA enforcement status: Ongoing

Brands named

inari medical oak canyoninariinari medical

UPCs

00850291007277

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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