PIPELINE FLEX EMBOLIZATION DEVICE recall in Canada: fracture risk
In plain language
This recall involves the PIPELINE FLEX EMBOLIZATION DEVICE sold in Canada. It's being recalled because the device may fracture or separate during use. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact Medtronic for further instructions.
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Affected products
PIPELINE FLEX EMBOLIZATION DEVICE
Model: More than 10 numbers, contact manufacturer.
Lot: All lots
Pipeline Flex Embolization Device with Shield Technology
Model: More than 10 numbers, contact manufacturer.
Lot: All lots
Why this matters
Fracture risk
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: More than 10 numbers, contact manufacturer.
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?
Fracture risk
What should consumers do?
Stop using the product immediately. Contact Medtronic 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?
Yes, there may be a health risk. Fracture risk
When was this product recalled?
This product was recalled on October 2, 2020.