Philips recalls AlluraXperFOlO/lO systems with System Code 722005 from 2003 to May 2011 due to potential monitor detachment causing injury risks.
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a Monitor Ceiling Suspension detaches from the actuator rotor shaft and the monitor falls, there is a risk of injury for the patient, user and bystander.
Philips is recalling AlluraXperFOlO/lO imaging systems with System Code 722005 that were sold between 2003 and May 2011. The monitor ceiling suspension could detach and fall, risking injury to patients, users, or bystanders.
The monitor ceiling suspension may detach from the actuator rotor shaft, causing the monitor to fall. This falling monitor poses a risk of injury to patients, users, and bystanders due to impact.
Healthcare facilities using these imaging systems from 2003 to May 2011 are affected. Patients, staff, and others near the monitor during operation are at risk of injury if the monitor falls.
Check for the System Code 722005 on the AlluraXperFOlO/lO imaging systems. These systems were sold between 2003 and May 2011 for vascular, cardiovascular, and neurovascular imaging.
Identify the System Code on the imaging system to confirm if it is 722005.
Reach out to Philips for guidance on next steps for affected systems.
Check if your AlluraXperFOlO/lO system has System Code 722005 and was purchased between 2003 and May 2011.
Contact Philips directly for instructions on how to handle the affected system.
Yes, if the monitor falls, it could injure patients, users, or bystanders.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3228-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3228-2018 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.
