Olympus recalls UHI-4 insufflation units after reports of air supply stopping when front panel LED turns off. Affected units have specific serial numbers; customers should contact Olympus for details.
Olympus has become aware of an increased trend of both repairs and customer complaints reporting "UHI-4 stopping air supply due to the front panel LED turning off".
Olympus is recalling its UHI-4 insufflation units after reports of air supply stopping when the front panel LED turns off. This issue could lead to equipment failure during medical procedures. Affected units have specific serial numbers and were sold through Olympus.
The front panel LED turning off can cause the unit to stop supplying air. This might lead to equipment failure during medical procedures if the issue occurs while the unit is in use. However, the problem appears to be a software or minor hardware issue rather than a critical safety hazard.
Medical professionals using Olympus UHI-4 insufflation units are most at risk. Patients receiving care during procedures using these units may also be affected.
Check for the model number UHI-4 on the unit. All units with serial numbers starting with 04953170324147 are affected. The recall covers all units sold by Olympus.
Look for the model number UHI-4 and serial numbers starting with 04953170324147 to confirm if your unit is affected.
Olympus has reported an increased trend of repairs and customer complaints about the UHI-4 stopping air supply when the front panel LED turns off.
Units with model number UHI-4 and serial numbers starting with 04953170324147 are affected. Check the unit's label for these details.
The recall does not specify a remedy, so contact Olympus directly for further instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1375-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1375-2024 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.
