Philips recalls INTEGRIS Allura 9 systems with specific model codes from 2003 to May 2011 due to risk of monitor detachment and injury to 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 certain INTEGRIS Allura 9 medical imaging systems that could have a monitor detach from its ceiling mount and fall, potentially injuring patients or users. This recall affects systems with specific model codes sold between 2003 and May 2011.
The monitor ceiling suspension may detach from the actuator rotor shaft, causing the monitor to fall. If the monitor falls, it could injure patients, users, or bystanders due to impact or collision.
Healthcare facilities using the recalled INTEGRIS Allura 9 systems from 2003 to May 2011 are most at risk, particularly during procedures where the monitor is suspended.
Check if your INTEGRIS Allura 9 system has a specific model code (722018) and was purchased between 2003 and May 2011 for cardiac imaging applications.
Identify if your system has the model code 722018 and was purchased between 2003 and May 2011.
Reach out to Philips for guidance on next steps for affected systems.
No, this recall applies only to medical facilities using the INTEGRIS Allura 9 systems.
Check if your system has model code 722018 and was purchased between 2003 and May 2011 for cardiac imaging applications.
Contact Philips for guidance on next steps for affected systems.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3213-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3213-2018 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.
