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Official recall record

Ingenia 3.0T

Health Canada — Medical Devices · 2024-09-13 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-09-13
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Philips has identified an issue in the MR system patient support where the integrated radio frequency (IRF) carrier assembly screws may come loose and protrude beyond the surface. This could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop movement. The IRF carrier, a component of the patient support within the MR system, supports the tabletop where the patient lies. As the patient moves into the MRI tunnel, the tabletop, supported by the IRF carrier, forms a container for positioning the posterior coil. Recall start date: September 4, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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