Guider Softip recall in Canada: Incorrect tip curve shape
In plain language
This recall involves Guider Softip and Guider Softip Xf guide catheters sold in Canada. They are being recalled because some units have an incorrect tip curve shape. This recall is for healthcare professionals.
What to do
- Contact the manufacturer, Boston Scientific Corporation, for additional information.
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Affected products
Guider Softip Xf
Model: H965100430, H965100440, M003101420, M003101430, M003101440, M003101620
Lot: More than 10 numbers, contact manufacturer.
Guider Softip
Model: M003100620, M003101620
Lot: More than 10 numbers, contact manufacturer.
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: H965100430, H965100440, M003100620, M003101420, M003101430, M003101440, M003101620
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 Guider Softip and Guider Softip Xf guide catheters sold in Canada. They are being recalled because some units have an incorrect tip curve shape. This recall is for healthcare professionals.
What should consumers do?
Contact the manufacturer, Boston Scientific Corporation, 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?
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 August 16, 2023.
Is the BOSTON SCIENTIFIC CORPORATION brand affected by this recall?
Yes, BOSTON SCIENTIFIC CORPORATION products are affected by this recall. This recall involves Guider Softip and Guider Softip Xf guide catheters sold in Canada. They are being recalled because some units have an incorrect tip curve shape. This recall is for healthcare professionals.