Medical Device Recalls
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1 result found
Recall Number: Z-2805-2020 |
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Results per Page |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| PVA, PREVENT is an FDA-authorized emergency ventilator designed to treat patients suffering from COV... | 2 | 08/14/2020 |
FEI # 3001151872 Precision Valve & Automation,Inc |
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