Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K032541 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
PoleStar system (N20 / N30) Warning Lamps Control Box, Warning Lamps Control Box Cables, Thermoflex ... | 2 | 07/06/2016 | Medtronic Navigation |
PoleStar FlexiCoil band D/E, revisions A and B, Catalog # 9733063, Usage: Low field MRI device u... | 2 | 08/19/2010 | Odin Medical Technologies Ltd. |
-