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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: EPIC INTERNATIONAL (THAILAND) CO., LTD SMARTEZ PUMP; PUMP, INFUSION, ELASTOMERIC

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EPIC INTERNATIONAL (THAILAND) CO., LTD SMARTEZ PUMP; PUMP, INFUSION, ELASTOMERIC Back to Search Results
Model Number SE0200-100
Device Problem Failure to Infuse (2340)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 12/01/2018
Event Type  malfunction  
Event Description
Smartez pump (se0200-100, lot# s8d33) containing zosyn 4.5 grams in 0.9% sodium chloride 100 ml is not infusing.Patient's picc line is flushing without problem.Site rn states that ed seems to drip fine when detached and unclamped.
 
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Brand Name
SMARTEZ PUMP
Type of Device
PUMP, INFUSION, ELASTOMERIC
Manufacturer (Section D)
EPIC INTERNATIONAL (THAILAND) CO., LTD
MDR Report Key8222084
MDR Text Key132492135
Report NumberMW5082857
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 01/03/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberSE0200-100
Device Lot Number S8D33
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/04/2019
Was Device Evaluated by Manufacturer? No Information
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
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