Philips recalls INTEGRIS Allura 15-12 (mono) 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 is recalling certain INTEGRIS Allura 15-12 (mono) medical imaging systems that could have a ceiling-mounted monitor fall if the suspension detaches. This poses a risk of injury to patients, users, or bystanders if the monitor falls.
The monitor ceiling suspension may detach from the actuator rotor shaft, causing the monitor to fall from the ceiling. If the monitor falls, it could injure patients, users, or bystanders.
Medical facilities using the recalled INTEGRIS Allura 15-12 systems from 2003 to May 2011 are affected. Patients and staff at these facilities are at risk if the monitor falls.
Check if your system has the model code 722043 and was purchased between 2003 and May 2011. The system is used for vascular, cardiovascular, and neurovascular imaging applications.
Verify your system's model code is 722043 and was purchased between 2003 and May 2011.
Reach out to Philips for guidance on next steps, as the recall remedy is not specified in the record.
No, this recall applies only to medical facilities using the INTEGRIS Allura 15-12 systems.
Contact Philips directly for guidance, as the recall remedy is not specified in the official notice.
The system was sold from 2003 to May 2011.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3216-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3216-2018 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.
