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EXACTAMIX H9382400-DYRecalls & reported problems

Baxter Healthcare Corporation · EXACTAMIX Compounder, EM2400 Display · Class 2

All models of EXACTAMIX (28)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05413765477584), received between Nov 13, 2019 and Nov 13, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 13, 2019Break; Break

    IT WAS REPORTED THERE WAS DAMAGE TO THE EXACTAMIX EM2400 DISPLAY MODULE CABLE AT THE CONNECTION TO THE DISPLAY. UPON SAMPLE RETURN, THE CABLE WAS OBSERVED TO HAVE EXPOSED WIRES. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

    Patient problems: No Patient Involvement

    MAUDE report 9315092 ↗

Other SYSTEM/DEVICE, PHARMACY COMPOUNDING devices

All SYSTEM/DEVICE, PHARMACY COMPOUNDING devices →

Sources and updates

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