Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K190592 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503; YelloPort Elite Hasson Adap... | 2 | 09/29/2022 | Surgical Innovations Ltd |
YelloPort Elite Universal Seal. For use in laparoscopic procedures. | 2 | 07/18/2022 | Surgical Innovations Ltd |
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