Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K221067 |
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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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| Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters, Medline Item Numbers: 40... | 2 | 03/26/2025 | MEDLINE INDUSTRIES, LP - Northfield |
| Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH 401600... | 1 | 09/26/2025 | Medline Industries, LP |
| Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electro... | 1 | 02/06/2026 | Medline Industries, LP |
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