Philips recalls Allura Xper FD1O C systems (2003-2011) due to potential monitor detachment causing injury. Affected users should contact Philips for details.
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 FD1O C imaging systems from 2003 to May 2011 because the ceiling-mounted monitor could detach and fall, risking injury to patients, users, or bystanders.
The ceiling suspension that holds the monitor may detach from its shaft, causing the monitor to fall. This fall could injure patients, users, or bystanders nearby due to the monitor's weight and size.
Healthcare facilities using Philips Allura Xper FD1O C systems with the FlexVision Monitor Ceiling Suspension 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 Philips Allura Xper FD1O C system has the FlexVision Monitor Ceiling Suspension installed. Systems were sold between 2003 and May 2011 for cardiac and vascular imaging.
Reach out to Philips for specific guidance on the recall and next steps.
No, this recall applies only to healthcare facilities using the imaging systems.
Check if your Philips Allura Xper FD1O C system with the FlexVision Monitor Ceiling Suspension was purchased between 2003 and May 2011.
Contact Philips directly for instructions on the recall and necessary actions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3225-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3225-2018 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.
