# FDA recall Z-3157-2024

> **MICROVENTION INC.** · Class II · device recall initiated 2024-08-05.

## Product

ERIC Retrieval Device  REF:  ER173020  ER174030  ER176044    The ERIC Retrieval Device is a mechanical thrombectomy device designed to restore blood flow by effectively removing clots from occlusive vasculature in patients suffering from acute ischemic stroke.

## Reason for recall

Due to Retrieval Device product labels stating the incorrect expiration dates that (5 years instead of 3 years) which extends beyond their true expiration date.

## Distribution

U.S. Nationwide distribution in the states of AR, CA, FL, IN, LA, MA, MN, MO, NC, NJ, NY, OH, PA, SC, TX and VA.

## Key facts

- **Recall number:** Z-3157-2024
- **Recalling firm:** MICROVENTION INC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-05
- **Report date:** 2024-09-25

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3157-2024

## Citation

> AI Analytics. FDA recall Z-3157-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-3157-2024. Source: US FDA. Licensed CC0.

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