Medical Device Recalls
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1 result found
Recall Number: Z-1246-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 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. |
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