Medical Device Recalls
-
|
11 to 13 of 13 Results
510(K) Number: K180086 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| 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 6-7-8. Indicated for endoscopic dilation of strictures of the esophagus ... | 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 |
-







