Medical Device Recalls
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1 result found
Recall Number: Z-1283-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC4... | 2 | 02/05/2026 |
FEI # 2429304 Olympus Corporation of the Americas |
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