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Home › FDA recalls › MicroScan Neg Multidrug Resistant MIC 1 REF C32368
CLASS II · ModerateFDA

Beckman Coulter, Inc. recalls MicroScan Neg Multidrug Resistant MIC 1 REF C32368

📅 Sep 8, 2025 · 📍 See notice
Recalling company
Beckman Coulter, Inc.
Product
MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried Gram Negative Breakpoint Combo Panels. MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.
Reason
Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Sep 8, 2025
Reported
Apr 15, 2026
Distribution
International distribution to the country of Poland.
Status
Ongoing
Quantity
3 boxes
Lot / codes
Catalog Number: C32368 UDI-DI code: 15099590720568 Lot Number: 2026-05-08
Company location
West Sacramento, CA
Recall type
Voluntary: Firm initiated
Recall number
Z-1794-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1794-2026 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.