Philips recalls Allura Xper FD series with software version 2.1.x for possible loose set screws causing monitors to fall, risking patient or user harm. Affected models include 722005-722028.
Set screws securing the two gliding rods of the Extra Monitors (called 7th and 8th monitor) mounted on the Monitor Ceiling Suspension (MCS) can come loose, the Extra monitors might disengage from the Mounting Ceiling Suspension structure and fall down, may lead to patient, user or service engineer harm that may require medical intervention.
Philips is recalling its Allura Xper FD series medical imaging devices with software version 2.1.x because set screws holding extra monitors to the ceiling can become loose. If these monitors detach, they could fall and cause injury to patients, users, or service technicians requiring medical attention.
The set screws that secure the extra monitors (7th and 8th monitors) to the ceiling suspension can become loose. If they detach, the monitors may fall, potentially causing injury to patients, users, or service engineers who could require medical intervention.
Healthcare facilities using Philips Allura Xper FD series with software version 2.1.x for vascular, cardiovascular, or neurovascular imaging are affected. Medical staff and patients using these devices are at risk of injury if the monitors fall.
Check for Philips Allura Xper FD series devices with software version 2.1.x. Affected models include 722005, 722006, 722008, 722010, 722012, 722013, 722025, 722026, 722027, 722028. US serial numbers starting with (01)00884838054202(21) or similar patterns.
Discontinue use of the affected Philips Allura Xper FD series devices with software version 2.1.x until a remedy is provided.
The affected models include Philips Allura Xper FD series with software version 2.1.x, specifically model numbers 722005, 722006, 722008, 722010, 722012, 722013, 722025, 722026, 722027, and 722028.
Set screws securing the extra monitors (7th and 8th monitors) to the ceiling suspension can become loose, potentially causing the monitors to fall and injure patients, users, or service engineers.
Check for software version 2.1.x on your Philips Allura Xper FD series device. Affected models include specific numbers like 722005-722028, and US serial numbers starting with patterns such as (01)00884838054202(21).
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0416-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0416-2022 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.
