Medical Device Recalls
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1 result found
510(K) Number: K141474 |
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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 Intelliport Medication Management System Sensor The system is indicated for use by healthcare ... | 2 | 03/08/2016 | Becton Dickinson & Company |
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