Philips recalls SmartPath to Ingenia El: X diagnostic devices due to loose screws that could block the horizontal tabletop, causing delays in diagnosis and patient anxiety.
Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may include anxiety of a patient is left on the tabletop inside the bore for a longer duration than anticipated. movement.
Philips is recalling its SmartPath to Ingenia Elition X diagnostic imaging devices because screws in the RF carrier assembly might become loose and protrude, potentially blocking the tabletop. This could delay diagnoses and cause patients to stay on the table longer than expected, leading to anxiety.
Loose screws in the RF carrier assembly can protrude beyond the surface, blocking the horizontal tabletop. This may cause delays in diagnosis and leave patients on the table longer than intended, increasing anxiety.
Healthcare professionals using the SmartPath to Ingenia Elition X for diagnostic imaging are most at risk. Patients using the device may experience longer wait times and anxiety.
The recalled product is the SmartPath to Ingenia Elition X, used for diagnostic imaging. It has serial numbers 85661 or 85676 and was sold with UDI-DI (01)00884838099746(21).
Look for serial numbers 85661 or 85676 on the device.
The integrated RF carrier assembly screws may become loose and protrude, potentially blocking the tabletop and causing delays in diagnosis or patient anxiety.
The recall record does not specify a remedy, so no action is required at this time.
The recall record does not mention a risk of serious injury, only potential delays in diagnosis and patient anxiety.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3205-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-3205-2024 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.
