Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K142749 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit, REF: T443952B, Pressure Monitoring Set, RX Only... | 2 | 06/25/2021 | Edwards Lifesciences, LLC |
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