8f Xcela Plus Implantable Ports & 8f Bioflo Plus Implantable Ports (2019-09-18)
In plain language
This recall involves 8f Xcela Plus and 8f Bioflo Plus Implantable Ports sold in Canada. They are being recalled because a component may not allow for a secure connection during implantation. This could delay the implantation procedure.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Follow the return or repair steps in the official notice.
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Affected products
8f Xcela Plus Implantable Ports
Model: H965440400
Lot: 5480564
8f Bioflo Plus Implantable Ports
Model: H965440140, H965440220
Lot: 5482424, 5487932, 5488008
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: 5480564, 5482424, 5487932, 5488008
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: H965440140, H965440220, H965440400
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?
This recall involves 8f Xcela Plus and 8f Bioflo Plus Implantable Ports sold in Canada. They are being recalled because a component may not allow for a secure connection during implantation. This could delay the implantation procedure.
What should consumers do?
Stop using the product immediately. Check model and lot numbers. Follow the return or repair steps in the official notice.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on January 10, 2020.