Medical Device Recalls
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1 result found
510(K) Number: K242376 |
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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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| Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Ballast Model/Catalog Number: M... | 1 | 10/24/2025 | BALT USA, LLC |
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