Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K213550 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002 | 2 | 10/13/2023 | Access Vascular, Inc |
| HydroPICC 5Fr Dual Lumen Maximal Barrier Kit, Product Model Number 80002004 | 2 | 10/13/2023 | Access Vascular, Inc |
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