Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K150735 |
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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 Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 1088452400... | 2 | 02/25/2020 | Covidien Llc |
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut an... | 2 | 03/18/2019 | Covidien, PLC |
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