Olympus High Flow Insufflation Unit recall: Issue with software algorithm which may lead to overpressure events
Issue with software algorithm which may lead to overpressure events.
The hazard: Fire or burn hazard
A fire or burn risk is what prompted this recall. Most of these incidents happen while the product is charging or left running unattended.
What the notice says: Issue with software algorithm which may lead to overpressure events.
Why it matters: The product can overheat, ignite or cause a burn. Where lithium batteries are involved the failure is fast and very hot, and water does not put it out quickly.
Symptoms and when to call a doctor
Treat a burn by cooling it under running water for about 20 minutes — not with ice, butter or ointment — and cover it loosely with a clean non-fluffy cloth. Get medical help for burns that are larger than the person’s palm, that are deep or white or charred, that involve the face, hands, feet or genitals, or any burn to a baby or young child. If someone has inhaled smoke and is coughing, hoarse or short of breath, call 911.
This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.
Recall details
- Recall number
- Z-1354-2026
- Published
- February 25, 2026
- Risk level
- Class I
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Olympus Corporation of the Americas
- Product type
- Medical devices
- Units affected
- 485 units
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Model Number: UHI-3; UDI-DI: 04953170140280, 04953170140297; All Serial Numbers.
- UPC codes
- 04953170140280, 04953170140297
Products covered by this recall
Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
Check your product
The notice names 4 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
UPC / barcode
Read the twelve digits under the barcode on the package.
- 04953170140280
- 04953170140297
Model or item number
On the rating label, the box or the instruction sheet.
- UHI-3
Serial number
On the rating plate, often next to the date of manufacture.
- s. — 485 units
Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Fire
Olympus Corporation of the Americas — A fire or burn risk is what prompted this recall. Most of these incidents happen while the product is charging or left running unattended.
- Stop using it and unplug it from the wall. If it runs on a battery pack, stop charging it.
- If it has already overheated, scorched or swelled, do not keep using it and do not try to repair it.
- Check that your smoke alarms work while you are thinking about it, and follow the remedy on this page.
- Move it off anything that burns — a bed, a sofa, a carpet, a pile of paper — and away from exits.
How the remedy works
CPSC recalls specify one of three remedies, and which one you get is not negotiable — but how smoothly it goes often is.
- A refund means the purchase price back, sometimes prorated by age for durable goods. Ask how they calculated it if the figure looks low.
- A replacement is usually the current model, not the recalled one. Confirm the replacement is not itself under recall.
- Several recalls now ask you to destroy the item and send a photo as proof. Register the claim before you do that, never after.
- Return shipping is the company’s cost. If you are asked to pay it, push back.
Company contact: Olympus Corporation of the Americas — 3500 Corporate Pkwy, Center Valley, PA, 18034-8229
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Olympus Corporation of the Americas medical devices recalled?
Issue with software algorithm which may lead to overpressure events. Issue with software algorithm which may lead to overpressure events.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: UPC 04953170140280, 04953170140297; model number UHI-3. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Stop using it and unplug it from the wall. If it runs on a battery pack, stop charging it.
Can I get my money back?
A refund means the purchase price back, sometimes prorated by age for durable goods. Ask how they calculated it if the figure looks low.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class II · 18 days ago
Olympus M3 Gold Autoclavable Foroblique Telescope 30 recall: There are identified discrepancies between the sterilization parameters
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in…
-
Class II · 18 days ago
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recall: While in the high-power operating mode, a video dropout/blackout may occur
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
-
Class II · 18 days ago
Olympus M3 Gold Autoclavable Lateral Telescope 70 recall: There are identified discrepancies between the sterilization parameters
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in…
-
Class II · 25 days ago
Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/ recall: Potential for detachment of ceramic tip due to manufacturing without
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
-
Class II · 25 days ago
Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/ recall: Potential for detachment of ceramic tip due to manufacturing without
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
-
Class II · 25 days ago
Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm recall: Potential for the inflation chart label affixed to the shaft of the device
Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm,