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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:182135

Alaris Auto ID Module Model 8600, a modular infusion pump and monitoring system

Official recall number

Z-2723-2020

Evidence summary

Product code
FRN
Recall status
Terminated
Event initiated
June 30, 2020
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2723-2020