Ih-Qc 3 recall in Canada: Medical device may give incorrect results
In plain language
This recall involves Ih-Qc 3, a medical device, sold in Canada. It's being recalled because it may produce incorrect test results. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Ih-Qc 3
Model: 009323
Lot: 08730 72 1 (SAP 709953 72 1)
Why this matters
Incorrect test results
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: 08730 72 1 (SAP 709953 72 1)
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 009323
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?
Incorrect test results
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?
Yes, there may be a health risk. Incorrect test results
When was this product recalled?
This product was recalled on May 3, 2022.
Is the Diamed Gmbh brand affected by this recall?
Yes, Diamed Gmbh products are affected by this recall. This recall involves Ih-Qc 3, a medical device, sold in Canada. It's being recalled because it may produce incorrect test results. Contact the manufacturer for more information.