OFFICIAL-SOURCE RECALL · CANADA
Direxion and Direxion HI-FLO Microcatheters Recall: Boston scientific is initiating the removal of
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Direxion and Direxion HI-FLO Microcatheters
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Boston scientific is initiating the removal of specific lots of Direxion and Direxion HI-FLO Microcatheters due to a manufacturing issue that may cause difficulty withdrawing the device from the carrier hoop and difficulty advancing or withdrawing the device through a guide catheter.
Hazard
Boston scientific is initiating the removal of specific lots of Direxion and Direxion HI-FLO Microcatheters due to a manufacturing issue that may cause difficulty withdrawing the device from the carrier hoop and difficulty advancing or withdrawing the device through a guide catheter.
Official recall notice
Direxion and Direxion HI-FLO Microcatheters
Agency: Health Canada
Official publication date: October 1, 2026
Read the official CANADA_MEDICAL_DEVICES recall notice →SCAN ONCE. KEEP WATCHING.
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