Olympus recalls EVIS EXERA II gastrointestinal videoscopes (GIF-HQ190 model) due to potential use of incorrect rubber part during repairs, which may not fit properly.
Part (A-rubber) intended for a different model of gastrointestinal videoscope may have been used when replacing part on GIF-HQ190 during the last repair at Olympus. An Incorrect A-rubber fits tighter on the GIF-HQ190 which would not meet the intended design specifications
Olympus is recalling specific EVIS EXERA II gastrointestinal videoscopes (GIF-HQ190 model) because an incorrect rubber part might have been used during repairs. This could cause the part to fit too tightly, potentially leading to improper function.
An incorrect rubber part (part A) may have been used during repairs for the GIF-HQ190 model. This part fits too tightly, which could lead to improper function but does not pose a direct risk of injury during normal use.
Medical professionals who own or use the recalled EVIS EXERA II gastrointestinal videoscopes (GIF-HQ190 model) are affected. Those who have had recent repairs with the incorrect part are at slightly higher risk.
Check for the model number GIF-HQ190 on the device. The serial numbers listed (2269931, 2611873, etc.) indicate the affected units. The device is intended for use in the upper digestive tract.
Identify the model number on the device, which should be GIF-HQ190 for affected units.
Reach out to Olympus Corporation of the Americas for further assistance or to confirm if your device is affected.
Olympus is recalling specific EVIS EXERA II gastrointestinal videoscopes (GIF-HQ190 model) because an incorrect rubber part may have been used during repairs, which could cause improper function.
The incorrect part may fit too tightly, potentially causing improper function but does not pose a direct risk of injury during normal use.
Check for the model number GIF-HQ190 and the listed serial numbers (2269931, 2611873, etc.) on your device.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1275-2022 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1275-2022 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.
