Philips recalls AIIuraXperFDlO monitors from 2003-2011 due to potential ceiling suspension detachment causing monitor falls and injury risks. Affected units may need repair or replacement.
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 certain AIIuraXperFDlO monitors made between 2003 and May 2011. The ceiling suspension that holds the monitor could detach, causing it to fall and potentially injure patients, users, or bystanders.
The ceiling suspension system that holds the monitor may detach from the actuator rotor shaft. If it detaches, the monitor could fall to the ground, posing a risk of injury to anyone nearby.
Healthcare facilities using these monitors for cardiac imaging or vascular procedures from 2003 to May 2011 are most at risk. Patients and staff during procedures could be injured if the monitor falls.
Check for the System Code 722010 on the monitor. Affected units were sold between 2003 and May 2011 for cardiac imaging applications.
Verify if your monitor has the System Code 722010 and was purchased between 2003 and May 2011.
Reach out to Philips for guidance on whether your monitor needs repair or replacement.
The System Code 722010 is the specific model for this recall.
These monitors were sold from 2003 to May 2011.
Check for the System Code 722010 and verify your purchase date was between 2003 and May 2011.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3229-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3229-2018 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.
