iVascular Sergeant recall in Canada: Performance issue
In plain language
This recall involves the iVascular Sergeant medical device sold in Canada. It's being recalled because the device's performance may be affected. Deterioration of the outer layer could lead to small pieces of material detaching. This recall is for healthcare professionals.
What to do
- Contact the manufacturer for additional information.
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Affected products
iVascular Sergeant
Model: DSPC18065001, DSPC18065002, DSPC18090001, DSPC18090002, DSPC18130001, DSPC18130002, DSPC18150001, DSPC18150002
Lot: All lots.
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: All lots.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: DSPC18065001, DSPC18065002, DSPC18090001, DSPC18090002, DSPC18130001, DSPC18130002, DSPC18150001, DSPC18150002
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 August 20, 2024.
Is the Life Vascular Devices Biotech S.L. brand affected by this recall?
Yes, Life Vascular Devices Biotech S.L. products are affected by this recall. This recall involves the iVascular Sergeant medical device sold in Canada. It's being recalled because the device's performance may be affected. Deterioration of the outer layer could lead to small pieces of material detaching. This recall is for healthcare professionals.