Medical Device Recalls
-
1 to 10 of 25 Results
510(K) Number: K051641 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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. |
-