Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K180086 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of strictures in the alime... | 2 | 01/31/2024 | Olympus Corporation of the Americas |
EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of strictures of the esophag... | 2 | 01/31/2024 | Olympus Corporation of the Americas |
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