Medical device recalls Moderate risk

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

Recall date
November 12, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0585-2026
FDA classification
Class II
Brand / firm
Remel, Inc
Sold / distributed
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.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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