Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K133532 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES... | 1 | 08/06/2021 | BioMedical Equipment Service Co (BMES) |
BD Alaris PCU REF 8015 | 1 | 11/07/2023 | CareFusion 303, Inc. |
BD Alaris Syringe Module, REF 8110 | 1 | 11/07/2023 | CareFusion 303, Inc. |
Alaris PCA Module 8120 | 1 | 11/07/2023 | CareFusion 303, Inc. |
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