Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K153193 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit ... | 2 | 03/29/2022 | InfuTronix LLC |
Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/med... | 2 | 07/23/2019 | InfuTronix LLC |
Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump | 1 | 05/21/2024 | OptumHealth Care Solutions LLC |
Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT107... | 1 | 03/28/2024 | InfuTronix LLC |
Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); ... | 1 | 03/28/2024 | InfuTronix LLC |
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