Medical Device Recalls
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1 result found
510(K) Number: K991501 |
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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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Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or re... | 1 | 05/01/2014 | Hospira Inc. |
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