# FDA recall Z-0002-2020

> **The Metrix Company** · Class II · device recall initiated 2018-09-21.

## Product

SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.

## Reason for recall

Potential for leaking product

## Distribution

US Nationwide distribution including the states of PA, MA, IL CA.

## Key facts

- **Recall number:** Z-0002-2020
- **Recalling firm:** The Metrix Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-09-21
- **Report date:** 2019-10-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dubuque, IA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0002-2020

## Citation

> AI Analytics. FDA recall Z-0002-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0002-2020. Source: US FDA. Licensed CC0.

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