Olympus Corporation of the Americas recalls
5 Olympus Corporation of the Americas recalls in our records. The latest: Olympus Corporation of the Americas recall: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable (Oct 7, 2026).
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| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 |  Olympus Corporation of the Americas recall: Olympus Tripp-Lite P580-025 25ft DisplayPort CableMedical devices · 543 cables | While in the high-power operating mode, a video dropout/blackout may occur when using a pa… Serious | FDA Class II |
| Oct 7, 2026 | Olympus Corporation of the Americas recall: Olympus M3 Gold Autoclavable Foroblique Telescope 30 and 1 more productMedical devices · 72 units; 50 units | There are identified discrepancies between the sterilization parameters listed in the Inst… Serious | FDA Class II |
| Sep 30, 2026 | Olympus Corporation of the Americas recall: Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11Medical devices · 305 units | Potential for the inflation chart label affixed to the shaft of the device to be incorrect… Serious | FDA Class II |
| Sep 30, 2026 | Olympus Corporation of the Americas recall: Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector and 3 more productsMedical devices · 404 units; 105 units; 2,142 units; 816 units | Potential for detachment of ceramic tip due to manufacturing without the designated amount… Serious | FDA Class II |
| Sep 2, 2026 | Olympus Corporation of the Americas recall: Powerseal 5 MMMedical devices · 335 units | Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-c… Serious | FDA Class II |
Olympus Corporation of the Americas recall questions
Is there a Olympus Corporation of the Americas recall right now?
The most recent Olympus Corporation of the Americas recall in our records: Olympus Corporation of the Americas recall: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, published by FDA on October 7, 2026.
How many Olympus Corporation of the Americas recalls have there been?
5 since September 2, 2026 in our records (5 medical devices), 0 of them in the most serious category.
How do I check if my Olympus Corporation of the Americas product is included?
Open the recall and compare the lot codes, UPCs, dates or model numbers with what you have; only the items listed are recalled.
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Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.