Philips recalls AlIura Xper F010 F monitors from 2003-2011 due to potential ceiling suspension detachment causing monitor falls. Affected units may cause injury to patients, users or bystanders.
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 AlIura Xper F010 F monitors produced between 2003 and May 2011. The ceiling suspension that holds the monitor could detach, causing it to fall and potentially injuring patients, users, or bystanders.
The ceiling suspension that holds the monitor may detach from the actuator rotor shaft. If it detaches, the monitor could fall to the ground, potentially causing injury to patients, users, or bystanders.
Healthcare facilities using the AlIura Xper F010 F monitors from 2003 to May 2011 are most at risk. Patients and staff in these facilities could be injured if the monitor falls.
Check for the AlIura Xper F010 F model with System Code 722002. The product was sold from 2003 through May 2011 for cardiac imaging applications.
Inspect the ceiling suspension for signs of detachment or damage.
Reach out to Philips for guidance on whether your monitor needs repair or replacement.
Check if your AlIura Xper F010 F monitor was purchased between 2003 and May 2011 for cardiac imaging use.
If the monitor falls, contact Philips immediately for assistance.
Philips does not provide a replacement; they recommend contacting them for guidance on repair or replacement options.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3226-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3226-2018 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.
