Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K031777 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Product is labeled in part: Inner Label "***S.M.A.R.T. Transhepatic Biliary Stent***REF Cat. No.***... | 2 | 05/10/2012 | Cordis Corporation |
Product is labeled in part: Inner Label "***SMART Control Transhepatic Biliary Stent***REF Cat. No.... | 2 | 05/10/2012 | Cordis Corporation |
S.M.A.R.T. CONTROL Transhepatic Biliary Stent. The Self-Expanding Nitinol Biliary Stent is delivere... | 2 | 02/15/2012 | Cordis Corporation |
-