Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K890328 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700... | 2 | 05/29/2018 | Gyrus Acmi, Incorporated |
| ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Rig... | 2 | 12/15/2023 | Olympus Corporation of the Americas |
| Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silicone ... | 2 | 07/21/2025 | Olympus Corporation of the Americas |
| Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The ... | 2 | 07/21/2025 | Olympus Corporation of the Americas |
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