Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K010060 |
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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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Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as... | 2 | 11/15/2019 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Talon Straight, 25 cm--Electrosurgical Device--RITA * Medical Systems, Inc. * StarBurst® Talon * * R... | 2 | 05/31/2006 | Rita Medical Systems, Inc. |
XLie with Tubing, 12 cm, Electrosurgical Device-RITA * Medical Systems, Inc. * StarBurst® Xli enhanc... | 2 | 05/31/2006 | Rita Medical Systems, Inc. |
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