Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K130904 |
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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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Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V... | 2 | 04/02/2015 | Medtronic Inc. Cardiac Rhythm Disease Management |
Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT81202... | 1 | 02/03/2015 | Covidien |
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