Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K896819 |
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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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TruWave with Vamp System Pressure monitoring set, REF: PXAVMP(3cc)/VAMP 68 in (173cm) PXAVMP3: x3... | 2 | 11/29/2023 | Edwards Lifesciences, LLC |
Pressure Monitoring sets with VAMP Plus closed blood sampling system model # T001691A, PXVP0566, PXV... | 2 | 04/18/2013 | Edwards Lifesciences, LLC |
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