Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K133532 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Alaris System PC Unit Model 8000 modular infusion pump and monitoring system | 1 | 08/06/2020 | CareFusion 303, Inc. |
Alaris System PC Unit Model 8015. modular infusion pump and monitoring system | 1 | 08/06/2020 | CareFusion 303, Inc. |
CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518) | 1 | 03/05/2020 | CareFusion 303, Inc. |
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. ... | 1 | 07/16/2019 | CareFusion 303, Inc. |
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