Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:192281

Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit IT1075-DUKE-HSP, IT1076-DUKE-HSP and IT1077-DUKE-HSP

Official recall number

Z-0832-2022

Evidence summary

Product code
FRN
Recall status
Open, Classified
Event initiated
October 19, 2021
Root cause
Employee error
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0832-2022