Philips recalls specific Integris-Allura X-ray systems due to potential oil leakage in cooling units, which may cause system shutdowns. Affected models include Integris CV Cesar-Powerpack-Visub-Nicol (722030) and others manufactured between Feb 2016 and May 2020.
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
Philips is recalling certain Integris-Allura X-ray systems because the cooling hoses may degrade over time, causing oil leaks that can lead to system shutdowns. This affects medical equipment used in hospitals and clinics, where proper functioning is critical for patient safety.
The deaeration hose in the X-ray tube cooling units may degrade over time, leading to oil leakage. This leakage can cause the system to automatically switch to low-dose fluoroscopy and display a warning message about tube cooler problems, which cannot be fixed by restarting the system.
Healthcare facilities using the recalled Integris-Allura X-ray systems are most at risk, as these devices are critical for medical imaging. Patients and staff using the affected equipment could experience interruptions in imaging services.
Check if your system has the model numbers listed: Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (722043), or other specific models manufactured between February 2016 and May 2020.
Identify your system model by checking the serial numbers or model codes listed in the recall notice.
Reach out to Philips Medical Systems Netherlands for assistance with the recall process.
The recall affects specific Integris-Allura X-ray systems including Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (722043), and other models manufactured between February 2016 and May 2020.
The deaeration hose in the X-ray tube cooling units may degrade over time, causing oil leakage that leads to system shutdowns and cannot be resolved by restarting the system.
Check your system model and contact Philips Medical Systems Netherlands for assistance with the recall process.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2229-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2229-2026 from Philips. 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.
