Medical Device Recalls
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1 result found
510(K) Number: K211738 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S... | 1 | 03/05/2025 | Bard Peripheral Vascular Inc |
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