# FDA recall Z-2573-2018

> **Diamedix Corporation** · Class III · device recall initiated 2018-01-05.

## Product

Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

## Reason for recall

Contains a gel-like contaminant that may affect product performance.

## Distribution

AZ, CA, FL, IL, IN, KY, MA, MI, MN, MO, NH, NJ, NY, OH, OK, PA, RI, TN, TX, and WI

## Key facts

- **Recall number:** Z-2573-2018
- **Recalling firm:** Diamedix Corporation
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-05
- **Report date:** 2018-08-08
- **Termination date:** 2019-11-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami Lakes, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2573-2018

## Citation

> AI Analytics. FDA recall Z-2573-2018. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-2573-2018. Source: US FDA. Licensed CC0.

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