5 results
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36ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a needle or a catheter.
FDA Recall
Terminated
·InfuTronix LLC·Product code FRN·May 28, 2019
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
FDA Recall
Open, Classified
·InfuTronix LLC·Product code FRN·October 19, 2021
Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
FDA Recall
Open, Classified
·InfuTronix LLC·Product code FRN·February 21, 2024
Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump and components
FDA Recall
Open, Classified
·InfuTronix LLC·Product code FRN·February 21, 2024
Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
FDA Recall
Open, Classified
·OptumHealth Care Solutions LLC·Product code FRN·April 18, 2024