Philips recalls Allura Xper FD2O Biplane systems with specific model codes from 2003 to May 2011 due to risk of monitor detachment causing injury to patients and users.
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 Allura Xper FD2O Biplane medical imaging systems with System Code 722013 that were sold between 2003 and May 2011. The monitor ceiling suspension could detach and fall, potentially injuring patients, users, or bystanders.
The monitor ceiling suspension that holds the large screen could detach from its mounting shaft. If it falls, it may cause injury to patients, users, or people nearby due to the monitor's weight and movement.
Healthcare facilities using the Allura Xper FD2O Biplane systems with System Code 722013 from 2003 to May 2011 are affected. Patients and staff during imaging procedures are at risk if the monitor falls.
Check if your system has System Code 722013 and was purchased between 2003 and May 2011. The device is used for cardiac imaging and vascular procedures.
Verify your system's code is 722013 and was purchased between 2003 and May 2011.
Reach out to Philips for guidance on next steps after confirming your system is affected.
No, only the Allura Xper FD2O Biplane systems with System Code 722013 from 2003 to May 2011.
The monitor could fall and cause injury to patients, users, or bystanders.
Check if your system has System Code 722013 and was purchased 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-3223-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3223-2018 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.
