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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:157839

Medfusion, Syringe Infusion Pump, Software Version V1.1, Rx Only, Manufactured by Smiths Medical ASD, Inc., 1500 Eureka Park, Lower Pemberton, Ashford, Kent, TN25 4BF, UK. In the administration of fluids requiring precisely controlled infusion rates including blood or blood products, lipids, drugs, antibiotics, enteral solutions and other therapeutic fluids.

Official recall number

Z-0313-2018

Evidence summary

Product code
FRN
Recall status
Terminated
Event initiated
August 22, 2017
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0313-2018

Field note

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