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Ingenia 3.0t

Official notice

13 Sept 2024

Last checked

13 Sept 2024

Medium riskHealth Canada

An official Health Canada notice concerns Ingenia 3.0t. 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 Published 2024-09-13.

What to do now

Contact the manufacturer if you require additional information.

Recall number

76041

Official notice

2024-09-13

The hazard

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

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

76041

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Affected products

Product 1

Affected products - Ingenia 3.0T, Lot or serial number - s/n: 34055, Model or catalogue number - 782103

Risk / hazard

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

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Philips, Ingenia 3.0t.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

76041

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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