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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BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring ... | 2 | 09/03/2020 | CareFusion 303, Inc. |
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120... | 1 | 09/04/2020 | CareFusion 303, Inc. |
CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518) | 1 | 03/05/2020 | CareFusion 303, Inc. |
PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY CASE FRONT W/KEYPAD 8015LS, TC100... | 1 | 09/04/2020 | CareFusion 303, Inc. |
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