# FDA recall Z-1556-2022

> **Micro Therapeutics,  Inc.** · Class II · device recall initiated 2022-06-30.

## Product

Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only

## Reason for recall

Outer carton packaging of microcatheters were exposed to wet substance during transport.

## Distribution

US Nationwide Distribution: None  OUS: Brazil

## Key facts

- **Recall number:** Z-1556-2022
- **Recalling firm:** Micro Therapeutics,  Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-30
- **Report date:** 2022-08-24

- **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-1556-2022

## Citation

> AI Analytics. FDA recall Z-1556-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1556-2022. Source: US FDA. Licensed CC0.

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