# FDA recall Z-0585-2026

> **Remel, Inc** · Class II · device recall initiated 2025-11-12.

## Product

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10    2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

## Reason for recall

Products may contain contamination, which may result in a darker or brown media color.

## Distribution

Worldwide - US Nationwide distribution in the states of AK, CA, FL, GA, IA, IL, IN, LA, MA, MD, ME, MI, MN, NE, NY, OH, OK, PA, RI, SD, TN, VA, WA, WI and the countries of Brazil, Canada, China, Cyprus, Finland, Great Britain, Ireland, Moldova, Norway, Singapore.

## Key facts

- **Recall number:** Z-0585-2026
- **Recalling firm:** Remel, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-12
- **Report date:** 2025-12-03

- **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-0585-2026

## Citation

> AI Analytics. FDA recall Z-0585-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0585-2026. Source: US FDA. Licensed CC0.

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