Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K210495 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR | 2 | 05/17/2023 | Surgical Innovations Ltd |
| YelloPort Elite, REF: EO0507005, 5x70 Optical Trocar, , Rx Only, SterileR | 2 | 05/17/2023 | Surgical Innovations Ltd |
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