Philips recalls Allura Xper FD10 and FD20 systems with monoplane fixed ceiling mounts due to risk of injury if the L-arm rotates and collides with hospital equipment.
Ceiling mounted L-arm contains a rotation cover that may potentially be susceptible to falling if a collision between the L-arm and other hospital equipment (i.e., an operating light) were to occur result in injury or potential sterility issues due to the cover becoming loose
Philips is recalling specific Allura Xper FD10 and FD20 systems with monoplane ceiling mounts because the rotating cover could fall if the system collides with other hospital equipment, potentially causing injury or sterility issues.
The ceiling-mounted L-arm has a rotation cover that might fall if it collides with other hospital equipment like operating lights. This could cause injury to staff or patients and compromise sterility in the operating room.
Hospital users who own or operate the recalled Philips Allura systems with monoplane fixed ceiling mounts are most at risk, particularly during surgical procedures where equipment collisions could occur.
Check for the model numbers listed: 722001 Allura Xper FD10C, 722003 Allura Xper FD10, 722006 Allura Xper FD20, and other specific models mentioned in the recall notice.
Identify the model number on your Philips Allura system to confirm if it is in the recall list.
Reach out to Philips customer support for further assistance with the recall.
The recall includes Philips Allura Xper FD10C (722001), Allura Xper FD10 (722003), Allura Xper FD20 (722006), and other specific models listed in the notice.
The recall does not specify a fix; affected users should contact Philips for guidance.
Check the model number on your Philips Allura system against the list of affected models provided in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0558-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0558-2024 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.
