Remel, Inc: Device Recall

Recall #Z-0585-2026 · 11/12/2025

Class II: Risk

Recall Details

Recall Number
Z-0585-2026
Classification
Class II
Product Type
Device
Recalling Firm
Remel, Inc
Status
Ongoing
Date Initiated
11/12/2025
Location
Lenexa, KS, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,000 US, 280 ROW

Reason for Recall

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

Product Description

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

Distribution Pattern

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.

Other Recalls by Remel, Inc

View all recalls by Remel, Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.