FDA Adverse Event Malfunction Summary report: N

SMART DOSE ELASTOMERIC INFUSION PUMP

MDR report key: 23333 · Received July 11, 1995

Report

Report Number
MW1006472
Event Type
Malfunction
Date Received
July 11, 1995
Date of Event
June 3, 1995
Report Date
June 27, 1995
Manufacturer
RIVER MEDICAL, INC.
Product Code
MEB
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

ELASTOMERIC PUMP WAS ACTIVATED, BUT THE MEDICATION WAS NOT DELIVERED TO THE PT. IT FAILED TO INFUSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SMART DOSE ELASTOMERIC INFUSION PUMP PUMP MEB RIVER MEDICAL, INC. 4120188, 4120201

Patients

Seq Age Sex Outcome Treatment
1 20 YR