Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K142323 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| GE Healthcare Vivid S60, ultrasound device | 2 | 07/10/2023 | GE Vingmed Ultrasound As |
| GE Healthcare Vivid S70, ultrasound device | 2 | 07/10/2023 | GE Vingmed Ultrasound As |
| GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW | 2 | 07/05/2024 | GE Vingmed Ultrasound As |
-







