Olympus recalls EVIS EXERA III Duodenoscope model TJF-Q190V due to recent reports of patient infections. Affected units include all serial numbers with specific UDI-DI code.
Recent reports of patient infection.
Olymp: Olympus is recalling its EVIS EXERA III Duodenoscope model TJF-Q190V after recent reports of patient infections. This recall affects all units with the specified serial numbers and UDI-DI code.
The recall is based on recent reports of patient infections linked to this specific duodenoscope model. The exact cause of infection is not specified in the recall notice.
Healthcare professionals using the Olympus EVIS EXERA III Duodenoscope model TJF-Q190V are likely affected. Patients undergoing procedures with this device may be at risk of infection.
Check for the model number TJF-Q190V on the device. All units with the UDI-DI code 04953170405563 and any serial number are affected.
Identify the model number on the device, which should be TJF-Q190V for affected units.
The recall is based on recent reports of patient infections linked to this specific model.
The recall notice does not specify a remedy, so contact Olympus directly for guidance.
Yes, affected units have the UDI-DI code 04953170405563 and any serial number.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2467-2023 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2467-2023 from Olympus. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
