Male External Catheter recall in Canada: Not sterile as labeled
In plain language
This recall involves Male External Catheters sold in Canada. They are being recalled because the labels incorrectly state they are sterile when they are not. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the lot number: 74B1801603 and model number: A1500.
- Contact Teleflex Medical for return instructions.
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Affected products
Male External Catheter
Model: A1500
Lot: 74B1801603
Why this matters
Risk of infection due to non-sterile product
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: 74B1801603
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: A1500
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?
Risk of infection due to non-sterile product
What should consumers do?
Stop using the product immediately. Check the lot number: 74B1801603 and model number: A1500. Contact Teleflex Medical for return instructions.
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. Risk of infection due to non-sterile product
When was this product recalled?
This product was recalled on March 15, 2019.