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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: B. BRAUN MELSUNGEN AG EASYPUMP ELASTOMERIC INFUSION PUMP 100ML - 200ML; PUMP, INFUSION, ELASTOMERIC

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B. BRAUN MELSUNGEN AG EASYPUMP ELASTOMERIC INFUSION PUMP 100ML - 200ML; PUMP, INFUSION, ELASTOMERIC Back to Search Results
Model Number 4540040-02
Device Problem Leak/Splash (1354)
Patient Problem Insufficient Information (4580)
Event Date 02/22/2023
Event Type  malfunction  
Event Description
During compounding in easypump 100ml - 200ml/hr size started leaking where the tubing connects to the easypump.Pump was discarded during compounding process.
 
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Brand Name
EASYPUMP ELASTOMERIC INFUSION PUMP 100ML - 200ML
Type of Device
PUMP, INFUSION, ELASTOMERIC
Manufacturer (Section D)
B. BRAUN MELSUNGEN AG
bethlehem PA 18018 3524
MDR Report Key16454108
MDR Text Key310586080
Report NumberMW5115289
Device Sequence Number1
Product Code MEB
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Pharmacist
Type of Report Initial
Report Date 02/23/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/27/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number4540040-02
Device Catalogue Number4540040-02
Device Lot Number22H05GE672
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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