Olympus recalls EVIS EXERA II Bronchovideoscopes (serial numbers) due to updated reprocessing instructions for chemicals and ETO sterilization. Affected users should contact Olympus for details.
Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization
Olymp: Olympus is recalling its EVIS EXERA II Bronchovideoscopes because of updated instructions for chemical reprocessing and ETO sterilization. This recall is important because improper use could lead to safety issues with the equipment.
The hazard involves potential risks from improper chemical reprocessing and ETO sterilization steps. If the reprocessing instructions are not followed correctly, it could lead to equipment damage or safety issues.
Healthcare professionals using the EVIS EXERA II Bronchovideoscopes are likely affected. Those who use the equipment for medical procedures are at the highest risk.
Check for the model name 'EVIS EXERA II Bronchovideoscope' and serial numbers listed in the recall notice. The unique device identifier (UDI) is 04953170339349.
Reach out to Olympus Corporation of the Americas for specific instructions on the recall and any necessary actions.
The model number is EVIS EXERA II Bronchovideoscope (BF-1TQ180).
Check the serial number and unique device identifier (UDI) listed in the recall notice. Affected units have the UDI 04953170339349.
Contact Olympus Corporation of the Americas for specific instructions on the recall and any necessary actions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1049-2022 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1049-2022 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.
