Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K173084 |
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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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Baxter Spectrum IQ Infusion Pumps, Product code 3570009. | 1 | 01/29/2022 | Baxter Healthcare Corporation |
Dose IQ Safety Software used with Spectrum IQ Infusion Pump | 1 | 08/11/2021 | Baxter Healthcare Corporation |
Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled ... | 1 | 08/06/2021 | Baxter Healthcare Corporation |
Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration o... | 2 | 04/23/2021 | Baxter Healthcare Corporation |
Infusion Pump | 2 | 02/25/2021 | Baxter Healthcare Corporation |
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software - Product Usage: intended to be used... | 2 | 12/23/2020 | Baxter Healthcare Corporation |
Spectrum IQ Infusion System with Dose IQ Safety Software | 1 | 10/22/2020 | Baxter Healthcare Corporation |
SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE, 3570009 | 2 | 10/13/2018 | Baxter Healthcare Corporation |
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