# FDA recall Z-1200-2025

> **Remel, Inc** · Class II · device recall initiated 2025-02-13.

## Product

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

## Reason for recall

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1200-2025
- **Recalling firm:** Remel, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-13
- **Report date:** 2025-02-26

- **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-1200-2025

## Citation

> AI Analytics. FDA recall Z-1200-2025. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-1200-2025. Source: US FDA. Licensed CC0.

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