Philips recalls certain cardiac imaging monitors from 2003-2011 that may detach and fall, risking injury. Affected units have System Code 722011. Stop using immediately if you own one.
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 cardiac imaging monitors with System Code 722011 made between 2003 and May 2011. The monitor ceiling suspension could detach and fall, potentially injuring patients, users, or bystanders.
The monitor's ceiling suspension system may detach from its mounting shaft, causing the large screen monitor to fall to the ground. This falling monitor could injure people in the immediate area, including patients and medical personnel.
Users of cardiac imaging monitors with System Code 722011 purchased between 2003 and May 2011 are affected. Patients, medical staff, and anyone nearby during use are at risk of injury.
Check for the System Code 722011 on your cardiac imaging monitor. The product was sold between 2003 and May 2011. This recall applies to all units with the FlexVision Monitor Ceiling Suspension.
Immediately stop using the monitor if it has System Code 722011 and was purchased between 2003 and May 2011.
The monitor's ceiling suspension may detach from its mounting shaft, causing it to fall and potentially injure patients, users, or bystanders.
System Code 722011.
Between 2003 and 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-3230-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3230-2018 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.
