beckman coulter, inc.medicalHigh PriorityActive

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.

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. was recalled because due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.. If you have this product, stop using it until you verify your lot or model details.

By RecallRadar Editorial Team

Sourced from FDA. Last verified April 20, 2026.

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Key facts

Date announced: April 15, 2026
Source agency: FDA

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

What's Being Recalled

Quoted source excerpt from the official notice.

Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand: Beckman coulter, inc.
Category: medical
Source agency: FDA
Announced: April 15, 2026
Country: US
Status: Active

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Catalog Number: C32368 UDI-DI code: 15099590720568 Lot Number: 2026-05-08

#	Model
1	Catalog Number: C32368 UDI-DI code: 15099590720568 Lot Number: 2026-05-08

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

1Stop using the affected product until you verify whether your item is impacted.
2Check the official recall notice and match your model, lot, or serial details.
3Follow the official instructions for repair, replacement, refund, or disposal.

Open Official Recall Notice

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: April 15, 2026
Last reviewed by RecallRadar: April 20, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists Catalog Number: C32368 UDI-DI code: 15099590720568 Lot Number: 2026-05-08.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the beckman coulter, inc. recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-1794-2026&limit=1

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