Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K870572 |
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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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Maximal Barrier Drape; Product Code: ASK-01000-UPMS | 2 | 05/30/2018 | Arrow International Inc |
ArrowClarke" PleuraSeal® Thoracentesis Kit | 2 | 04/03/2018 | Arrow International Inc |
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