Flexible Intubation Endoscopes recall in Canada: Improper sterilization
In plain language
This recall involves Flexible Intubation Endoscopes sold in Canada. They are being recalled due to incorrect sterilization instructions. Healthcare professionals should stop using the product and follow the updated instructions from the manufacturer.
What to do
- Stop using the product immediately.
- Contact the manufacturer for updated sterilization instructions.
- Check model numbers if provided.
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Affected products
Flexible Intubation Endoscopes
Model: 11301AA1, 11301BN1, 11301BND1, 11301BNX, 11302BD2, 11302BDD2, 11302BDX, 11303BNX
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Improper sterilization
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: 11301AA1, 11301BN1, 11301BND1, 11301BNX, 11302BD2, 11302BDD2, 11302BDX, 11303BNX
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?
Improper sterilization
What should consumers do?
Stop using the product immediately. Contact the manufacturer for updated sterilization instructions. Check model numbers if provided.
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. Improper sterilization
When was this product recalled?
This product was recalled on August 28, 2020.