Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K051641 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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. |
The Alaris PC Unit, Model 8015 (manufactured or serviced between April 2008 and January 2009). Th... | 1 | 08/03/2009 | Cardinal Health 303 dba Cardinal Health |
The Alaris PC Unit, Model Numbers 8000 and 8015 (formerly Medley PC Unit) software version 8 and abo... | 1 | 08/03/2009 | Cardinal Health 303 dba Cardinal Health |
The Alaris PC Unit, Model Numbers 8000 and 8015 (formerly Medley PC Unit) with software version 4 an... | 1 | 08/03/2009 | Cardinal Health 303 dba Cardinal Health |
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