Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K220263 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe Curved Cat ... | 2 | 02/04/2026 |
FEI # 3013002167 Vortex Surgical Inc. |
| Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4 Illuminated Flex-Tip VK... | 2 | 02/04/2026 |
FEI # 3013002167 Vortex Surgical Inc. |
| Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25; | 2 | 12/30/2025 |
FEI # 3013002167 Vortex Surgical Inc. |
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