Reported Jan 28, 2026 · Ongoing

Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog Number: MFM-CMS Product Description: MFM-CMS is…

Edan Diagnostics

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Edan Diagnostics · 9833 Pacific Heights Blvd · San Diego, CA · 92121-4707

Is this the product you have?

  • Brand NameEDAN
  • Product NameCentral
  • Monitoring System Model/Catalog NumberMFM-CMS
  • Product DescriptionMFM-CMS is a central monitoring system product, which can connect and manage information from EDAN medical devices. MFM-CMS offers central management for monitoring information from the medical devices. All these collected information can be displayed, printed, alarmed and recorded
  • ComponentNo
Lot codes and dates
  • EDAN ModelMFM-CMS
  • UDI-DI code06944413800229
  • Serial/Lot Numbers

    159 of 159 codes

    • 261432-M18312480001
    • 261432-M18803430001
    • 261432-M18B04070001
    • 261432-M18B04070002
    • 261432-M18C06730001
    • 261432-M18C06730002
    • 261432-M18C06730004
    • 261432-M18C06730003
    • 261432-M18C06730005
    • 261432-M18C06730006
    • 261432-M19402160001
    • 261432-M19402160003
    • 261432-M19402160002
    • 261432-M19B02530001
    • 261432-M19B02530006
    • 261432-M19A10370007
    • 261432-M19B02530005
    • 261432-M19B02530003
    • 261432-M19B02530002
    • 261432-M20213550006
    • 261432-M20213550005
    • 261432-M20213550003
    • 261432-M20213550002
    • 261432-M20213550004
    • 261432-M20213550001
    • 261432-M20702060001
    • 261432-M20702060006
    • 261432-M20702060002
    • 261432-M20702060004
    • 261432-M20702060007
    • 261432-M20702060005
    • 261432-M20708340003
    • 261432-M20708340005
    • 261432-M20708340002
    • 261432-M20708340004
    • 261432-M20708340001
    • 261432-M20708340006
    • 261432-M20810650003
    • 261432-M20810650004
    • 261432-M20810650002
    • 261432-M20810650001
    • 261432-M20810650006
    • 261432-M20810650005
    • 261432-M18401960001
    • 261432-M20C04930001
    • 261432-M20C04930002
    • 261432-M20C04930005
    • 261432-M20C04930004
    • 261432-M20C04930003
    • 261432-M20C04930006
    • 261432-M21111490005
    • 261432-M21111490004
    • 261432-M21111490003
    • 261432-M21111490002
    • 261432-M21111490006
    • 261432-M21111490001
    • 261432-M21206490002
    • 261432-M21206490006
    • 261432-M21206490001
    • 261432-M21206490005
  • EDAN ModelMFM-CMS
  • UDI-DI code06944413814264
  • Serial/Lot Numbers
    • 262237-M24611330012
    • 262237-M24611330001
    • 262237-M24611330011
    • 262237-M24611330014
    • 262237-M24611330009
    • 262237-M24611330019
    • 262237-M24611330004
    • 262237-M24611330008
    • 262237-M24611330007
    • 262237-M24611330017
    • 262237-M24611330010
    • 262237-M24611330003
    • 262237-M24611330005
    • 262237-M24611330015
    • 262237-M24611330013
    • 262237-M24611330018
    • 262237-M24611330002
    • 262237-M24611330006
    • 262237-M24611330016
    • 262237-M24814380001
    • 262237-M24905030001
    • 262237-M24C17400001
    • 262237-M24C17400003
    • 262237-M24C17400004
    • 262237-M24C17400002
    • 262237-M24C17400005
    MRM-CMSIII
    • 262237-M24B06940008
    • 262237-M24B06940001
    • 262237-M24B06940003
    • 262237-M24B06940005
    • 262237-M24B06940010
    • 262237-M24B06940004
    • 262237-M24B06940007
    • 262237-M24B06940006
    • 262237-M24B06940002
    • 262237-M24B06940009
Amount recalled
195

This recall covers 16 products

The agency filed one notice per product. You are reading one of them; the other 15 are below.

3 more are in the archive.

Where it was sold

Why it was recalled

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.