BriteBlade Pro recall in Canada: components may separate
In plain language
This recall involves BriteBlade Pro Fiber Optic Systems sold in Canada. It's being recalled because components in the laryngoscope blade may become loose and separate. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and lot numbers.
- Return the product as instructed by the manufacturer.
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Affected products
BriteBlade Pro Single-Use Fiber Optic Mac 3
Model: 040-713U
Lot: 181000113, 181100001, 181200005
Laryngoscope BrightBlade Pro Fibre Optic - Miller 2
Model: 040-722U
Lot: 181000115
BritePro Solo Fibre Optic Laryngoscope Handle With Batteries and Blade
Model: 040-333U
Lot: 180900072, 180900104, 181100097, 181200024
Why this matters
Components may separate from the 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: 180900072, 180900104, 181100097, 181200024, 181000113, 181100001, 181200005, 181000115
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 040-333U, 040-713U, 040-722U
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?
Components may separate from the device
What should consumers do?
Stop using the product immediately. Check the model and lot numbers. Return the product as instructed by the manufacturer.
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. Components may separate from the device
When was this product recalled?
This product was recalled on October 11, 2019.
Is the BriteBlade Pro brand affected by this recall?
Yes, BriteBlade Pro products are affected by this recall. This recall involves BriteBlade Pro Fiber Optic Systems sold in Canada. It's being recalled because components in the laryngoscope blade may become loose and separate. Stop using the product and follow the return steps in the official notice.