Philips recalls Allura Xper F020 Biplane DR Tables (2003-2011) with potential monitor detachment risk. Affected units may cause patient or user injury if monitor falls from ceiling suspension.
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 Biplane DR Tables made between 2003 and May 2011. The monitor ceiling suspension could detach and fall, risking injury to patients, users, or bystanders.
The monitor ceiling suspension may detach from the actuator rotor shaft during use. If it falls, it could hit patients, users, or bystanders causing injury.
Healthcare professionals using the table for vascular, cardiovascular, or neurovascular imaging are most at risk. Patients and others nearby could also be injured if the monitor falls.
Check for the Allura Xper F020 Biplane DR Table with System Code 722020. The product was sold between 2003 and May 2011 for vascular, cardiovascular, and neurovascular imaging applications.
Inspect the ceiling suspension for signs of detachment or damage before use.
The recall applies to Allura Xper F020 Biplane DR Tables with System Code 722020 sold between 2003 and May 2011 for vascular, cardiovascular, and neurovascular imaging. Check your model and purchase date.
If the monitor falls, stop using the table immediately and seek medical attention for anyone injured.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3236-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-3236-2018 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.
