Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K922391 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1 | 2 | 06/20/2019 | Stryker GmbH |
Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2056-1 | 2 | 06/20/2019 | Stryker GmbH |
-