Philips recalls Allura Xper F010/10 DRTable models from 2003 to May 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 Allura Xper F010/10 DRTable models produced between 2003 and May 2011. The monitor ceiling suspension could detach and fall, risking injury to patients, users, or bystanders.
The monitor ceiling suspension may detach from the actuator rotor shaft, causing the large screen monitor to fall to the ground. If the monitor falls, it can injure patients, users, or bystanders due to impact.
Healthcare facilities using the Allura Xper F010/10 DRTable for vascular, cardiovascular, or neurovascular imaging from 2003 to May 2011 are affected. Patients and staff during procedures are at risk of injury if the monitor falls.
Check for the Allura Xper F010/10 DRTable with System Code 722019. The product was sold from 2003 to May 2011 for vascular, cardiovascular, and neurovascular imaging applications.
Inspect the ceiling suspension for signs of detachment or damage before use.
No, this recall applies only to medical facilities using the Allura Xper F010/10 DRTable for imaging procedures.
The product was sold from 2003 to May 2011.
System Code 722019 for the Allura Xper F010/10 DRTable.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3235-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3235-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
