Medical Device Recalls
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1 result found
510(K) Number: K924610 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 1) Adult Manual Resuscitator, 2K8004, Oxygen Reservoir Bag, Adult Mask; 2) Adult Manual Resuscitat... | 2 | 08/13/2013 | Carefusion 2200 Inc |
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