Remel, Inc recalls 1. CAMHB W/LHB
- Recalling company
- Remel, Inc
- Product
- 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
- Reason
- Products may contain contamination, which may result in a darker or brown media color.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Nov 12, 2025
- Reported
- Dec 3, 2025
- 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.
- Status
- Ongoing
- Quantity
- 1,000 US, 280 ROW
- Lot / codes
- 1. UDI-DI 848838018831, lots 305529, 311228, 316019, 320993 2. UDI-DI 848838091353, lot 317287
- Company location
- Lenexa, KS
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0585-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0585-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.