D-100 HBA1C Hemoglobin Testing System recall in Canada: liquid waste leak
In plain language
This recall involves the D-100 HBA1C Hemoglobin Testing System sold in Canada. It's being recalled because a pump failure could cause a leak of liquid waste containing diluted patient samples. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
D-100 HBA1C Hemoglobin Testing System
Model: 290-1000
Lot: All serial numbers
Why this matters
Exposure to diluted patient samples
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: All serial numbers
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 290-1000
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?
Exposure to diluted patient samples
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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. Exposure to diluted patient samples
When was this product recalled?
This product was recalled on December 10, 2018.