Medical Device Recalls
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1 to 10 of 25 Results
510(K) Number: K051641 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BD Alaris Syringe Module, REF 8110 | 1 | 11/07/2023 | CareFusion 303, Inc. |
| BD Alaris PCU REF 8015 | 1 | 11/07/2023 | CareFusion 303, Inc. |
| Alaris PCA Module 8120 | 1 | 11/07/2023 | CareFusion 303, Inc. |
| CareFusion Alaris PCA Module, Model 8120 | 1 | 03/05/2020 | CareFusion 303, Inc. |
| CareFusion Alaris Syringe Module, Model 8110 | 1 | 03/05/2020 | CareFusion 303, Inc. |
| CareFusion Alaris Pump Module, Model 8100 | 1 | 03/05/2020 | CareFusion 303, Inc. |
| Alaris PC Unit, Model 8015 | 2 | 06/19/2017 | CareFusion 303, Inc. |
| Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power suppl... | 2 | 03/21/2017 | CareFusion 303, Inc. |
| Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitor... | 2 | 06/28/2016 | CareFusion 303, Inc. |
| Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power su... | 2 | 05/04/2016 | CareFusion 303, Inc. |
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