Fotofinder ATBM Master recall in Canada: Unauthorized device
In plain language
This recall involves the Fotofinder ATBM Master, a medical device. It's being recalled because it is an unauthorized device in Canada. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Specific affected products are listed in the official notice.
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves the Fotofinder ATBM Master, a medical device. It's being recalled because it is an unauthorized device in Canada. Healthcare professionals should contact the manufacturer for more information.
What should consumers do?
Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on March 3, 2025.
Is the Fotofinder Systems, Inc brand affected by this recall?
Yes, Fotofinder Systems, Inc products are affected by this recall. This recall involves the Fotofinder ATBM Master, a medical device. It's being recalled because it is an unauthorized device in Canada. Healthcare professionals should contact the manufacturer for more information.