# FDA recall Z-2257-2018

> **Quantimetrix Corporation** · Class III · device recall initiated 2017-12-21.

## Product

Dropper Plus Point-of-Care Urinalysis Dipstick Control kit    The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine by the listed test methods, and as a control for confirmatory tests such as K-CHECK and Ictotest reagent tablets, and for hCG methods.

## Reason for recall

The kits contained an incorrect lot of Dropper Plus Level 1 vials

## Distribution

US Distribution to the state of : Kansas

## Key facts

- **Recall number:** Z-2257-2018
- **Recalling firm:** Quantimetrix Corporation
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-21
- **Report date:** 2018-06-27
- **Termination date:** 2021-01-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Redondo Beach, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2257-2018

## Citation

> AI Analytics. FDA recall Z-2257-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-2257-2018. Source: US FDA. Licensed CC0.

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