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EASYPUMP 4540044-02Recalls & reported problems

B. Braun Medical Inc. · Easypump® ST 50-1-S · Class 2

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 04046964449000), received between May 22, 2018 and May 22, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inaccurate Flow Rate” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Inaccurate Flow Rate1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionMay 22, 2018Inaccurate Flow Rate; Inaccurate Flow Rate

    AS REPORTED BY THE USER FACILITY (TRANSLATION OF USER FACILITY INFORMATION BY BBM SALES ORGANIZATION IN FRANCE): PUMP-FLOW RATE-FAST

    Patient problems: No Information

    MAUDE report 7535402 ↗

Other PUMP, INFUSION, ELASTOMERIC devices

All PUMP, INFUSION, ELASTOMERIC devices →

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