MediFlo MDC270050Recalls & reported problems
Ndc Homecare LLC · MEDIFLO 270ML VOL/5ML HR 24/CS · Class 2
Data updated Oct 16, 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 00850007185022), received between Feb 1, 2024 and Feb 1, 2024 — classified as 1 malfunction.
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 16, 2026.
Reports received per month
Most reported problems
Patient problems
- Chemical Exposure1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 1, 2024
MIDDLE-AGED MALE WITH HISTORY OF GASTROHEPATIC LYMPHADENOPATHY. PROCEDURE: CHEMO TREATMENT PER 5FU BALL. PATIENT (PT) WAS RECEIVING 5FU TREATMENT PER BALL AND WAS OVER 24 HOURS INTO TREATMENT. PT WAS SLEEPING AND WHEN AWOKE, NOTICED THAT THE ELASTOMERIC BALL WAS LEAKING. PATIENT PLACED A PLASTIC BAG AROUND BALL AND CAME TO INFUSION THERAPY. INFUSION THERAPY REPORTED THAT THE BALL WAS EMPTY. IT WAS NOT KNOWN THE AMOUNT OF MEDICATION WAS RECEIVED. PATIENT¿S AREAS OF EXPOSURE WERE CLEANED AND CLOTHING DISCARDED. UNKNOWN HARM TO PATIENT AT THIS TIME. MANUFACTURER RESPONSE FOR PUMP, INFUSION, ELASTOMERIC, MEDIFLO (PER SITE REPORTER). REPORTED BY PHARMACIST.
Patient problems: Chemical Exposure
MAUDE report 18621365 ↗
Other Pump, Infusion, Elastomeric devices
- EASYPUMP 4540018-02B. Braun Medical Inc. · PUMP, INFUSION, ELASTOMERIC313 reports
- Halyard 13568Avanos Medical, Inc. · PUMP, INFUSION, ELASTOMERIC86 reports
- ON-Q* Pain Relief System with SELECT-A-FLOW 13472Avanos Medical, Inc. · Pump, infusion, elastomeric73 reports
- Halyard 13472Avanos Medical, Inc. · PUMP, INFUSION, ELASTOMERIC68 reports
- EASYPUMP 4540008-02B. Braun Medical Inc. · PUMP, INFUSION, ELASTOMERIC54 reports
- DOSI-FUSER L25915-500D1-USALeventon Sau · Pump, Infusion, Elastomeric1 recall0 reports
- DOSI-FUSER L25915-600D1-USALeventon Sau · Pump, Infusion, Elastomeric1 recall0 reports
- Halyard 13561Avanos Medical, Inc. · PUMP, INFUSION, ELASTOMERIC42 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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