Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K101843 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Angiodynamics® DuraMax® 15.5F x 36 cm Chronic Hemodialysis Catheter Set (With Cuff 31cm from Tip) --... | 2 | 01/12/2012 |
FEI # 3008319439 Angiodynamics Worldwide Headquarters |
| Angiodynamics® DuraMax® 15.5F x 28 cm Chronic Hemodialysis Catheter Set (with Cuff 23cm from Tip) --... | 2 | 01/12/2012 |
FEI # 3008319439 Angiodynamics Worldwide Headquarters |
| Angiodynamics® DuraMax® 15.5F x 24 cm Chronic Hemodialysis Catheter Set (with Cuff 19cm from Tip) --... | 2 | 01/12/2012 |
FEI # 3008319439 Angiodynamics Worldwide Headquarters |
| Angiodynamics® DuraMax® 15.5F x 22 cm Chronic Hemodialysis Catheter Set (with Cuff 17cm from Tip) --... | 2 | 01/12/2012 |
FEI # 3008319439 Angiodynamics Worldwide Headquarters |
| Angiodynamics® DuraMax® 15.5F x 32 cm Chronic Hemodialysis Catheter Set (with Cuff 27cm from Tip) --... | 2 | 01/12/2012 |
FEI # 3008319439 Angiodynamics Worldwide Headquarters |
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