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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| DURAMAX STACKED TIP 24CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining Long-Term vascular ... | 2 | 05/03/2024 |
FEI # 1319211 Angiodynamics, Inc. |
| DURAMAX STACKED TIP 28CM STR. BASIC KIT, 1-UP PG- Indicated for use in attaining Long-Term vascular ... | 2 | 05/03/2024 |
FEI # 1319211 Angiodynamics, Inc. |
| DURAMAX STACKED TIP 28CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining Long-Term vascular ... | 2 | 05/03/2024 |
FEI # 1319211 Angiodynamics, Inc. |
| DURAMAX STACKED TIP 32CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining Long-Term vascular ... | 2 | 05/03/2024 |
FEI # 1319211 Angiodynamics, Inc. |
| DuraMax Chronic Hemodialysis Catheter, REF: H787103028015/A, H787103028025/A, H787103028031/A, H7871... | 1 | 03/26/2026 |
FEI # 1721504 Merit Medical Systems, Inc. |
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