Philips recalls INTEGRIS Allura 9 F FDXD systems with specific model codes from 2003 to May 2011 due to risk of monitor ceiling suspension detaching 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 recalls certain INTEGRIS Allura 9 F FDXD medical imaging systems from 2003 to May 2011. The monitor ceiling suspension could detach and fall, risking injury to patients, users, or bystanders.
The monitor ceiling suspension may detach from its mounting mechanism, causing the large screen monitor to fall to the ground. This falling monitor poses a risk of injury to anyone nearby, including patients, medical staff, and bystanders.
Healthcare facilities using the affected INTEGRIS Allura 9 F FDXD systems 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 722497 and was purchased between 2003 and May 2011. The affected systems are used for cardiac imaging and vascular procedures.
Identify if your INTEGRIS Allura 9 F FDXD system has the model code 722497 and was purchased between 2003 and May 2011.
Reach out to Philips customer support for guidance on next steps if your system is affected.
The monitor ceiling suspension could detach from the actuator rotor shaft, causing the monitor to fall and potentially injure patients, users, or bystanders.
Check if your system has the model code 722497 and was purchased between 2003 and May 2011. Contact Philips for further instructions.
The recall record does not specify a fix or remedy; affected users should contact Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3219-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3219-2018 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.
