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Philips mr system breast coil
Official notice
15 Nov 2024
Last checked
15 Nov 2024
An official Health Canada notice concerns Philips mr system breast coil. Philips has identified an issue with patient set up while using the MR system breast coil where, if the cross-section of the prone patient, breast coil, and patient table exceeds the internal diameter of the magnet bore, the patient may be compressed between the breast coil and top of the magnet bore potentially resulting in harm to the patient. Recall start date: November 7, 2024 Published 2024-11-15.
What to do now
Contact the manufacturer if you require additional information.
Recall number
76517
Official notice
2024-11-15
The hazard
The hazard
Philips has identified an issue with patient set up while using the MR system breast coil where, if the cross-section of the prone patient, breast coil, and patient table exceeds the internal diameter of the magnet bore, the patient may be compressed between the breast coil and top of the magnet bore potentially resulting in harm to the patient. Recall start date: November 7, 2024
How to check if you're affected
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
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Philips.
Source & status
Source & status
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Category
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Recall details
Recall details
Recall number
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Source tier
Documents, notices & source
See the official notice and source documents for full details.
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