# FDA recall Z-2587-2024

> **Inari Medical - Oak Canyon** · Class I · device recall initiated 2024-07-19.

## Product

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

## 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.

## Distribution

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.

## Key facts

- **Recall number:** Z-2587-2024
- **Recalling firm:** Inari Medical - Oak Canyon
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-19
- **Report date:** 2024-08-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2587-2024

## Citation

> AI Analytics. FDA recall Z-2587-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2587-2024. Source: US FDA. Licensed CC0.

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