Medical Device Recalls
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1 result found
Recall Number: Z-0022-2026 |
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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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| NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154. ... | 2 | 10/02/2025 |
FEI # 3005467144 Northeast Scientific Inc. |
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