Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K113526 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Codman Certas Programmable Valve In Line Valve with SiphonGuard Device, Catheter and Accessories Pr... | 2 | 01/29/2014 | Codman & Shurtleff, Inc. |
Codman Certas Programmable Valve In Line Valve only with SiphonGuard Device Product Code: 82-8804 ... | 2 | 01/29/2014 | Codman & Shurtleff, Inc. |
Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal Catheter and Accessories Pro... | 2 | 01/29/2014 | Codman & Shurtleff, Inc. |
Codman Certas Programmable Valve In Line Valve with Catheter and Accessories Product Code: 82-8801 ... | 2 | 01/29/2014 | Codman & Shurtleff, Inc. |
Codman Certas Programmable Valve In Line Valve Only Product Code: 82-8800 Product Usage: The C... | 2 | 01/29/2014 | Codman & Shurtleff, Inc. |
Codman Certas Programmable Valve In Line Valve with SiphonGuard Device, Unitized Bactiseal Catheter ... | 2 | 01/29/2014 | Codman & Shurtleff, Inc. |
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