Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K170317 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels | 3 | 01/17/2023 | Abbott Laboratories |
Alinity i Total Beta-hCG Reagent Kit, List Number 07P5121 | 2 | 12/22/2018 | Abbott Ireland Diagnostics Division |
-