Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K121675 |
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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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25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in a Tyvek/Mylar double... | 2 | 10/18/2016 | Synergetics Inc |
25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator, Product/Part Number 70025SP... | 2 | 10/18/2016 | Synergetics Inc |
25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator, Product/Part Number 70025S, package... | 2 | 10/18/2016 | Synergetics Inc |
25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS r... | 2 | 10/18/2016 | Synergetics Inc |
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