Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071574 |
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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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MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire & Echo Needle 4F. A sheath used to fac... | 2 | 10/07/2016 | Argon Medical Devices, Inc |
Greatbatch Stiffer Coaxial Micro-Introducer. Model #/ Name: 10904-001 Stiffer Coaxial Micro-Introduc... | 2 | 11/18/2016 | Greatbatch Medical |
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