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MULTI-AD® 513501Recalls & reported problems

B. Braun Medical Inc. · MULTI-AD® Fluid Dispensing System · Class 1

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 04022495770387), received between Mar 6, 2020 and Mar 6, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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

  • Contamination /Decontamination Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionMar 6, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY: CUSTOMER IDENTIFIED ANOTHER PARTICLE IN AN AMPICILLIN/SULBACTAM 40MG/ML DILUTION. CUSTOMER STATED THAT THEY HAVE CONTINUED TO FIND SMALL PARTICLES DILUTION BAGS. SOME TECHNICIANS STATED THAT THEY ONLY CAN SEE THESE PARTICLES IN THE BAG AFTER A DAY OR TWO FROM INITIAL PRODUCTION. NO INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9800841 ↗

Other DISPENSER, LIQUID MEDICATION devices

All DISPENSER, LIQUID MEDICATION devices →

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