SIGNA™ Architect recall in Canada: Hearing impairment risk
In plain language
This recall involves the SIGNA™ Architect medical device sold in Canada. It's being recalled because it can produce elevated acoustic noise during scanning, which could lead to hearing impairment. Contact the manufacturer if you require additional information.
What to do
- Contact the manufacturer for more information.
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Affected products
SIGNA™ Architect
Model: SIGNA ARCHITECT
Lot: 905684MR3T
Why this matters
Hearing impairment risk
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 905684MR3T
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SIGNA ARCHITECT
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Hearing impairment risk
What should consumers do?
Contact the manufacturer for more 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?
Yes, there may be a health risk. Hearing impairment risk
When was this product recalled?
This product was recalled on November 7, 2024.
Is the Ge Medical Systems LLC brand affected by this recall?
Yes, Ge Medical Systems LLC products are affected by this recall. This recall involves the SIGNA™ Architect medical device sold in Canada. It's being recalled because it can produce elevated acoustic noise during scanning, which could lead to hearing impairment. Contact the manufacturer if you require additional information.