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Kaluza C Perpetual Education LicenseRecalls & reported problems

Beckman Coulter, Inc. · Kaluza C Perpetual Education License · Class 1

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Sep 17, 2018Terminated

    Compatibility issue between the software and Microsoft updates to Windows 7, 8, and 10. The compatibility issue causes the software to be unusable which could result in a delay of reporting results.

    Z-1982-2019 · Root cause: Software Manufacturing/Software Deployment · FDA record ↗

Other Calculator/Data Processing Module, For Clinical Use devices

All Calculator/Data Processing Module, For Clinical Use devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.