Philips recalls AIIura Xper F010 DR Tables with System Code 722022 from 2003-2011 due to risk of monitor detachment and falling, potentially injuring patients or 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 AIIura Xper F010 DR Tables with System Code 722022 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, which holds a large screen monitor, may detach from the actuator rotor shaft. If it detaches, the monitor can fall to the ground, potentially causing injury to patients, users, or bystanders.
Healthcare facilities using the AIIura Xper F010 DR Table with System Code 722022 from 2003 to May 2011 are affected. Patients and staff during imaging procedures are at risk of injury if the monitor falls.
Check for the System Code 722022 on the AIIura Xper F010 DR Table. The product was sold between 2003 and May 2011 for vascular, cardiovascular, and neurovascular imaging applications.
Inspect the monitor ceiling suspension for signs of detachment or damage.
Reach out to Philips for guidance on whether the table needs repair or replacement.
The recall applies to AIIura Xper F010 DR Tables with System Code 722022 sold between 2003 and May 2011. Check your system code to see if it's affected.
If the monitor falls, stop using it immediately and contact Philips for assistance. The recall addresses the risk of detachment, not an actual incident.
Philips does not provide a specific replacement process in this recall notice. Contact them directly for options.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3231-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3231-2018 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.
