Medical Device Recalls
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26 to 29 of 29 Results
Product: alaris Class 1 Recall Date from: 01/01/2020 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518) | 1 | 03/05/2020 | CareFusion 303, Inc. |
CareFusion Alaris PCA Module, Model 8120 | 1 | 03/05/2020 | CareFusion 303, Inc. |
CareFusion Alaris Pump Module, Model 8100 | 1 | 03/05/2020 | CareFusion 303, Inc. |
CareFusion Alaris Syringe Module, Model 8110 | 1 | 03/05/2020 | CareFusion 303, Inc. |
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