United StatesMicroScan Neg Multidrug Resistant MIC 1, REF C32368 (UDI‑DI 15099590720568), Lot 2026-05-08, catalog number C32368, is the affected product; it is for use with MicroScan dried gram-negative MIC/combo and breakpoint combo panels to determine antimicrobial susceptibility and/or identification of aerobic and facultatively anaerobic gram-negative bacilli. The product was recalled due to a manufacturing issue (incorrectly processing) with the in vitro multidrug resistant test; three boxes were distributed internationally to Poland.
What's being recalled
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.
Recalling firm: Beckman Coulter, Inc., West Sacramento, CA, United States.
How to identify it
Catalog Number: C32368 UDI-DI code: 15099590720568 Lot Number: 2026-05-08
The hazard
Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
International distribution to the country of Poland.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
Canada