Philips recalls Allura Xper F020 DR Tables (System Code 722023) from 2003-2011 where the monitor ceiling suspension may detach, risking injury to patients and users. Affected units have specific model codes and were sold in cardiac imaging applications.
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 Allura Xper F020 DR Tables with System Code 722023 that were sold between 2003 and May 2011. The monitor ceiling suspension could detach and fall, potentially injuring patients, users, or bystanders during cardiac imaging procedures.
The monitor ceiling suspension may detach from the actuator rotor shaft, causing the monitor to fall. This fall could injure patients, users, or bystanders during cardiac imaging procedures.
Healthcare professionals using cardiac imaging equipment and patients undergoing procedures with these tables are most at risk. The recall applies to specific models sold between 2003 and May 2011.
Check for the System Code 722023 on the Allura Xper F020 DR Table. These units were sold between 2003 and May 2011 for cardiac imaging applications.
Inspect the monitor ceiling suspension for signs of detachment or damage.
Yes, if your Allura Xper F020 DR Table has System Code 722023 and was purchased between 2003 and May 2011.
Look for System Code 722023 on the table and confirm it was sold between 2003 and May 2011 for cardiac imaging applications.
Inspect the monitor ceiling suspension for detachment or damage. If you find issues, contact Philips for further guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3232-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3232-2018 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.
