# FDA recall Z-0209-2018

> **Remel Inc** · Class II · device recall initiated 2017-11-02.

## Product

CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.

## Reason for recall

Product may have incorrect cation information detailed on the product label.

## Distribution

Distribution was made to AL, MD, ME, NC, and TN.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-0209-2018
- **Recalling firm:** Remel Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-02
- **Report date:** 2017-12-13
- **Termination date:** 2020-08-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lenexa, KS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0209-2018

## Citation

> AI Analytics. FDA recall Z-0209-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0209-2018. Source: US FDA. Licensed CC0.

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