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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K153193
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Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump 1 05/21/2024 FEI # 3009456923
OptumHealth Care Solutions LLC
Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); ... 1 03/28/2024 FEI # 3011581906
InfuTronix LLC
Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit ... 2 03/29/2022 FEI # 3011581906
InfuTronix LLC
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