Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K060339 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Mahurkar" Elite Acute Dual Lumen Catheter Tray, Straight Extensions with IC* Safety Components, 12 F... | 2 | 09/01/2015 | Covidien LLC |
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