---
title: "MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 1509959072056... — FDA record Z-1794-2026 | Is It on Recall"
description: "Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test."
url: https://isitonrecall.com/recall/fda-device-z-1794-2026-microscan-neg-multidrug-resistant-mic-1-ref-c32368-udi-di-code-15099590720568-intended-use-for-use-w/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For use with MicroScan D... — FDA record Z-1794-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 8, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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
- **Recalling firm**: Beckman Coulter, Inc.
- **Quantity**: 3 boxes
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1794-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1794-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Catalog Number: C32368 UDI-DI code: 15099590720568 Lot Number: 2026-05-08 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

International distribution to the country of Poland.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Apr 15, 2026
- **Recall initiation date**: Sep 8, 2025
- **Center classification date**: Apr 8, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1794-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Beckman Coulter Inc. records](https://isitonrecall.com/brand/beckman-coulter-inc/)