Female Luer Lock recall in Canada: particulate may enter fluid path
In plain language
This recall involves Female Luer Lock medical devices sold in Canada. It's being recalled because removing the dust cap may generate particulate that could enter the fluid path. If particulate enters the bloodstream, it could cause allergic reactions, infection, or tissue damage.
What to do
- Stop using the product immediately.
- Contact the manufacturer for more information.
- Follow the return or disposal instructions from the manufacturer.
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Affected products
Female Luer Lock
Model: BC693
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Internal injury from particulate matter
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: BC693
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?
Internal injury from particulate matter
What should consumers do?
Stop using the product immediately. Contact the manufacturer for more information. Follow the return or disposal instructions from 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. Internal injury from particulate matter
When was this product recalled?
This product was recalled on September 28, 2018.