Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K043299 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120... | 1 | 09/04/2020 | CareFusion 303, Inc. |
Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System modules built on or befo... | 2 | 06/10/2008 | Cardinal Health 303 Inc DBA Alaris Products |
U9 Socket Integrated Circuit ("U9 IC") on the display board of the following Alaris System modules b... | 2 | 06/10/2008 | Cardinal Health 303 Inc DBA Alaris Products |
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