# FDA recall Z-1085-2024

> **Stryker, Inc.** · Class II · device recall initiated 2023-12-06.

## Product

Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm

## Reason for recall

The microcatheter IFU contains an intended use that has not been evaluated by the FDA.

## Distribution

US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.

## Key facts

- **Recall number:** Z-1085-2024
- **Recalling firm:** Stryker, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-06
- **Report date:** 2024-02-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1085-2024

## Citation

> AI Analytics. FDA recall Z-1085-2024. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1085-2024. Source: US FDA. Licensed CC0.

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