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The official notice did not include a photo. Check the product details and identifiers below.
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An official Health Canada notice concerns Siemens biograph mmr system. Siemens Healthcare GmbH became aware of this issue as part of a customer complaint investigation. It has been identified that this issue can occur when certain parameters (Echo spacings 0.50 MS; 0.51 MS, and 0.52 MS) are used in EPI (Echo-Planar Imaging), sequences will excite high internal stress inside the gradient coil assembly. This may lead to cracks and damage to the gradient coil. Recall start date: March 15, 2024 Published 2024-03-22.
What to do now
Contact the manufacturer if you require additional information.
Recall number
75287
Official notice
2024-03-22
The hazard
The hazard
Siemens Healthcare GmbH became aware of this issue as part of a customer complaint investigation. It has been identified that this issue can occur when certain parameters (Echo spacings 0.50 MS; 0.51 MS, and 0.52 MS) are used in EPI (Echo-Planar Imaging), sequences will excite high internal stress inside the gradient coil assembly. This may lead to cracks and damage to the gradient coil. Recall start date: March 15, 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: Siemens.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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