Getinge 88-Series Washer- Disinfector recall: Potential for device to overheat during operation if the circulation pressure
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.
The hazard: Fire or burn hazard
This product can overheat or catch fire, which is why the instruction is to unplug and stop using it rather than to keep an eye on it.
What the notice says: Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.
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-0016-2026
- Published
- October 8, 2025
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Getinge Disinfection Ab
- Product type
- Medical devices
- Units affected
- 902 units
- Distribution
- Nationwide
- Made in
- Sweden
- Lot / code info
- Model Number: 88-5. UDI-DI Numbers: 07340153700109, 07340153700116. Software Version: GD 14080 Rev A. All Lot Numbers with electrical heating.
- UPC codes
- 07340153700109
Products covered by this recall
Getinge 88-Series Washer- Disinfector. Model Number: 88-5.
Check your product
The notice names 1 code 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.
- 07340153700109
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
Getinge Disinfection Ab — This product can overheat or catch fire, which is why the instruction is to unplug and stop using it rather than to keep an eye on it.
- Stop using it and unplug it from the wall. If it runs on a battery pack, stop charging it.
- Move it off anything that burns — a bed, a sofa, a carpet, a pile of paper — and away from exits.
- Do not leave it charging overnight or while the house is empty while you wait for the remedy.
- If it has already overheated, scorched or swelled, do not keep using it and do not try to repair it.
Claiming your refund, repair or replacement
The recalling company decides the remedy and funds it. You should never pay for a recall repair or for return shipping.
- Use the company contact on this page first. Most firms run a dedicated recall page with a claim form that is far quicker than their main support line.
- If the company stops responding, escalate to the CPSC. Firms under a recall order have reporting duties to the agency.
- Have the model number, the date code and your photos ready. Many companies issue store credit by default — ask for cash or a card reversal if you would rather have it.
- No receipt? Say so. Recall refunds are routinely paid without proof of purchase, because the hazard is what triggers the obligation.
Company contact: Getinge Disinfection Ab — Ljungadalsgatan 11, Vaxjo
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 Getinge Disinfection Ab medical devices recalled?
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered. Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: UPC 07340153700109. 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?
Use the company contact on this page first. Most firms run a dedicated recall page with a claim form that is far quicker than their main support line.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class II · 11 days ago
Stryker Sustainability Solutions Bard EP XT Decapolar Steerable recall: Diagnostic electrophysiology (EP) catheter may have a breached sterile
Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could…
-
Class II · 11 days ago
Steris Corporation Verify Biological Steam Test Pack Model/ recall: Geobacillus stearothermophilus spore population in affected products may fall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam…
-
Class II · 11 days ago
Medtronic MiniMed, Inc. Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin recall: Some MiniMed Flex insulin pumps were released with missing (i.e
Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed…
-
Class II · 11 days ago
Philips Medical Systems Spectral CT and Spectral CT 7500 RT recall: Software issues may affect the safety and performance of Spectral CT
Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or…
-
Class II · 11 days ago
Medline Industries, LP Rollator, Bariatric, Basic Steel, Blue recall: The front fork stem bolt/wheel assembly may disconnect from the rollator
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from…
-
Class II · 11 days ago
Onkos Surgical Inc. My3D recall: Personalized pelvic implants inadvertently mixed up and distributed
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.