Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K223041 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| RENASYS EDGE The RENASYS® EDGE pump is indicated for patients who would benefit from a suction pu... | 2 | 11/22/2024 | Smith & Nephew Medical, Ltd. |
| RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction... | 2 | 04/18/2024 | Smith & Nephew Medical, Ltd. |
| RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction... | 2 | 04/18/2024 | Smith & Nephew Medical, Ltd. |
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