Versacross Connect LAAC Access Solution recall in Canada: performance issue
In plain language
This recall involves the Versacross Connect LAAC Access Solution sold in Canada. It's being recalled because the guidewire may get stuck in the dilators. This is a health product recall for healthcare professionals.
What to do
- Contact the manufacturer for additional information.
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Affected products
Versacross Connect LAAC Access Solution
Model: VXAK0007
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Performance issue
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: VXAK0007
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?
Performance issue
What should consumers do?
Contact the manufacturer for additional information.
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. Performance issue
When was this product recalled?
This product was recalled on October 16, 2023.
Is the Baylis Medical Company Inc. brand affected by this recall?
Yes, Baylis Medical Company Inc. products are affected by this recall. This recall involves the Versacross Connect LAAC Access Solution sold in Canada. It's being recalled because the guidewire may get stuck in the dilators. This is a health product recall for healthcare professionals.