Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K924529 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Rese... | 2 | 12/20/2016 | Medtronic Inc |
Medtronic Custom Perfusion Tubing Pack, Rx, Sterile EO. Terumo Cardiovascular Systems (Terumo CVS... | 3 | 02/26/2016 | Medtronic Perfusion Systems |
-