# FDA recall Z-3240-2017

> **The Metrix Company** · Class II · device recall initiated 2017-09-13.

## Product

SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,

## Reason for recall

The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as ordered and as labeled on the inner and outer boxes.

## Distribution

AZ, MA, IL, FL

## Key facts

- **Recall number:** Z-3240-2017
- **Recalling firm:** The Metrix Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-13
- **Report date:** 2017-10-11
- **Termination date:** 2018-05-25

- **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-3240-2017

## Citation

> AI Analytics. FDA recall Z-3240-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-3240-2017. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
