Olympus Corporation of the Americas Recall
Olympus Corporation of the Americas is recalling Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed …
Olympus Corporation of the Americas
Olympus Corporation of the Americas Recalls (2026)
Every recall we are tracking for Olympus Corporation of the Americas, newest first, sourced from the FDA. If you are wondering whether your Olympus Corporation of the Americas product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new Olympus Corporation of the Americas recall posts.
6 recalls · updated Jan 29, 2026
Olympus Corporation of the Americas Recall
Olympus Corporation of the Americas is recalling Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number:KD-VC433Q-0730; …
Olympus Corporation of the Americas
Olympus Corporation of the Americas Recall
Olympus Corporation of the Americas is recalling Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0725; …
Olympus Corporation of the Americas
Olympus Corporation of the Americas Recall
Olympus Corporation of the Americas is recalling Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.. …
Olympus Corporation of the Americas
Olympus Corporation of the Americas Recall
Olympus Corporation of the Americas is recalling Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic …
Olympus Corporation of the Americas
Olympus Corporation of the Americas Recall
Olympus Corporation of the Americas is recalling Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S. Hazard: Firm is initiating a removal due to …
Olympus Corporation of the Americas
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