Medical Device Recalls
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1 result found
510(K) Number: K981035 |
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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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Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF... | 3 | 09/19/2018 | Smiths Medical ASD Inc. |
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