Inari Medical - Oak Canyon: Medical Device Recall in 2024 - (Recall #: Z-2587-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class I

Date Initiated: July 19, 2024

Date Posted: August 28, 2024

Recall Number: Z-2587-2024

Event ID: 95069

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 2488

Code Information:

UDI-DI:00850291007277. All lots. IU-01011 REV. C.

Distribution Pattern:

Worldwide - US Nationwide distribution including in the states of PA, FL, GA, CA, IL, SC, NY, MN, UT, TN, WI, MI, KS, SD, AZ, AR, IN, KY, TX, AL, MS, DE, MA, OH, MO, WV, VA, NC, NV, CO, NE, OR, NM, NH, NJ, CT, ID, IA, WA, MD, OK, RI, DC, PR, LA, ND, VT and the countries of New Zealand, Chile, Australia.

Voluntary or Mandated:

Voluntary: Firm initiated