Philips recalls Allura Xper FD2O imaging systems with specific model codes from 2003-2011 due to risk of monitor detachment causing injury. 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 Allura Xper FD2O imaging systems that could have a ceiling-mounted monitor detach and fall, risking injury to patients, users, or bystanders. This recall affects systems with specific model codes sold between 2003 and May 2011.
The ceiling-mounted monitor suspension system may detach from its shaft, causing the monitor to fall to the ground. If the monitor falls, it could injure patients, users, or bystanders nearby.
Healthcare facilities using Philips Allura Xper FD2O imaging systems with the specified model code from 2003 to May 2011 are most at risk. Patients and staff during imaging procedures could be injured if the monitor falls.
Check if your system has the model code 722006 and was purchased between 2003 and May 2011 for cardiac imaging applications. The system includes an actuator for the FlexVision Monitor Ceiling Suspension.
Identify if your Philips Allura Xper FD2O system has model code 722006 and was purchased between 2003 and May 2011.
Reach out to Philips for guidance on next steps for affected systems.
The ceiling-mounted monitor suspension may detach from its shaft, causing the monitor to fall and potentially injure patients, users, or bystanders.
Check if your system has model code 722006 and was purchased between 2003 and May 2011. Contact Philips for guidance.
Yes, if the monitor falls, there is a risk of injury to 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-3221-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3221-2018 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.
