Medical Device Recalls
-
21 to 21 of 21 Results
510(K) Number: K012842 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Ventlab, LLC V-Care manual resuscitators with integrated manometer, multiple accessory configuration... | 2 | 11/21/2023 | SunMed Holdings, LLC |
-