Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K971923 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer. | 1 | 12/23/2025 | Draeger, Inc. |
| Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer. | 1 | 12/23/2025 | Draeger, Inc. |
-







