IGEA Fast recall in Canada: Unlicensed medical device
In plain language
This recall involves the IGEA Fast Multistandard System and its components sold in Canada. It's being recalled because the device's license expired and was not renewed, and its components lack proper identification. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for return instructions.
- Do not dispose of the product without guidance.
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Affected products
IGEA Fast Multistandard System
Model: IG4500B
Lot: More than 10 numbers, contact manufacturer.
IGEA Fast Probe
Model: 04.01.001
Lot: More than 10 numbers, contact manufacturer.
IGEA Fast Probe Support
Model: 04.01.002
Lot: More than 10 numbers, contact manufacturer.
IGEA Fast Power Supply
Model: 31949
Lot: More than 10 numbers, contact manufacturer.
IGEA Fast Gel Pad
Model: 40129
Lot: More than 10 numbers, contact manufacturer.
IGEA Fast Orange Ring
Model: 10529
Lot: More than 10 numbers, contact manufacturer.
IGEA Fast Vaporizer
Model: 10537
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Unlicensed medical device
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 04.01.001, 04.01.002, 10529, 10537, 31949, 40129, IG4500B
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?
Unlicensed medical device
What should consumers do?
Stop using the product immediately. Contact the manufacturer for return instructions. Do not dispose of the product without guidance.
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. Unlicensed medical device
When was this product recalled?
This product was recalled on January 8, 2018.
Is the IGEA Fast brand affected by this recall?
Yes, IGEA Fast products are affected by this recall. This recall involves the IGEA Fast Multistandard System and its components sold in Canada. It's being recalled because the device's license expired and was not renewed, and its components lack proper identification. Stop using the product and follow the return steps in the official notice.