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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:210742

Z-800 Infusion System. Model/Catalog Number: Z-800, Z-800F, Z-800W, Z-800WF. The Z-800 Infusion system is intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient under the direction or supervision of a physician or other certified healthcare professional.

Official recall number

Z-0506-2025

Evidence summary

Product code
FRN
Recall status
Open, Classified
Event initiated
October 18, 2024
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0506-2025

Field note

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