Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K952516 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Portex Anaerobic Pulsator Arterial Blood Sampling Kit, with Liquid Sodium Heparin for Gases and Elec... | 3 | 01/29/2015 |
FEI # 1217052 Smiths Medical ASD, Inc. |
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