Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K790071 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
A20975A "Working insert, with ramp, one way" (Lots 13ZW to 172W; A20976A "Bridge, one way" (Lots 146... | 2 | 02/23/2018 | Olympus Corporation of the Americas |
High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used ... | 2 | 06/26/2017 | Olympus Corporation of the Americas |
Olympus Trocar Spikes, Model numbers: A5821, A5948, A5949, WA58341L, and WA58343L Used in conjunc... | 2 | 03/18/2010 | Olympus America Inc. |
-