Medical Device Recalls
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1 result found
510(K) Number: K070712 |
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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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| Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures. | 2 | 09/29/2022 |
FEI # 3002808173 Surgical Innovations Ltd |
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