Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K031741 |
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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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Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933 | 2 | 08/30/2019 | CareFusion 303, Inc. |
Alaris EtCO2 Module, Model 8300. A capnograph that continuously monitors end tidal carbon dioxide (... | 2 | 12/21/2015 | CareFusion 303, Inc. |
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