Olympus recalls UHI-4 High Flow Insufflation Units due to potential unexpected display shutdowns causing air delivery to stop. Affected units have specific serial numbers and model numbers.
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
Olympus is recalling its UHI-4 High Flow Insufflation Units because the front panel display may turn off unexpectedly, stopping air delivery. This could lead to interrupted medical procedures if the device is used during surgery or critical care.
The front panel display may turn off unexpectedly, causing the air delivery system to stop working. This could interrupt critical medical procedures like surgery or patient care where continuous air supply is needed. The risk is primarily for medical settings where the device is used.
Medical professionals using Olympus UHI-4 units for insufflation during procedures are most at risk. Patients receiving care from these devices may also be affected if the unit stops delivering air unexpectedly.
Check for the model number UHI-4 on the device. Affected units have specific serial numbers listed in the recall notice: 04953170324147 and 04953170467219. All units with this model number are included in the recall.
Look for the model number UHI-4 on the device to confirm it is affected.
This recall applies to Olympus UHI-4 High Flow Insufflation Units used in medical procedures. If your device has the model number UHI-4, it is affected.
Check for the model number UHI-4 and the specific serial numbers listed: 04953170324147 or 04953170467219. All units with this model number are included.
The recall does not specify a remedy, so no action is required beyond checking if your device is affected. Contact Olympus for further guidance if needed.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2776-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2776-2026 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.
