Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K133532 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. ... | 1 | 07/16/2019 | CareFusion 303, Inc. |
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