TactiCath Quartz recall in Canada: Loss of contact force information
In plain language
This recall involves the TactiCath Quartz Contact Force Ablation Catheter sold in Canada. It's being recalled because of a high rate of reported complaints for loss of contact force information during use. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers PN-004 065 and PN-004 075.
- Contact Abbott for further instructions.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
TactiCath Quartz
Model: PN-004 065, PN-004 075
Lot: Not applicable
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: Not applicable
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: PN-004 065, PN-004 075
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 the TactiCath Quartz Contact Force Ablation Catheter sold in Canada. It's being recalled because of a high rate of reported complaints for loss of contact force information during use. Stop using the product and follow the return steps in the official notice.
What should consumers do?
Stop using the product immediately. Check model numbers PN-004 065 and PN-004 075. Contact Abbott for further 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?
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 June 12, 2020.