Philips recalls INTEGRIS Allura 15-12 (biplane) 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 (biplane) medical imaging systems that could have a ceiling-mounted monitor detach and fall, risking injury to patients, users, or bystanders.
The monitor ceiling suspension may detach from its mounting shaft, causing the monitor to fall to the ground. This could injure patients, users, or bystanders if the monitor falls during medical procedures.
Medical facilities using the recalled INTEGRIS Allura 15-12 systems from 2003 to May 2011 are most at risk, particularly during procedures where the monitor is suspended.
Check for the system code 722044 on the INTEGRIS Allura 15-12 (biplane) systems. These systems were sold between 2003 and May 2011 for vascular, cardiovascular, and neurovascular imaging applications.
Look for the system code 722044 on the INTEGRIS Allura 15-12 (biplane) system.
Reach out to Philips for guidance on next steps if you have the recalled system.
The monitor ceiling suspension may detach from its mounting shaft, causing the monitor to fall and potentially injure patients, users, or bystanders.
INTEGRIS Allura 15-12 (biplane) systems with system code 722044 sold between 2003 and May 2011.
Check for the system code 722044 on the INTEGRIS Allura 15-12 (biplane) system. These systems were sold between 2003 and May 2011 for vascular, cardiovascular, and neurovascular imaging applications.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3217-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3217-2018 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.
