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Vectorflow antegrade catheterization product
Official notice
23 Apr 2026
Last checked
23 Apr 2026
An official Health Canada notice concerns Vectorflow antegrade catheterization product. Teleflex has initiated a voluntary recall for certain lots of the above-mentioned products due to receipt of a supplier-initiated recall of the Merit 16f dual-valved splittable sheath introducer component, which is included in impacted arrow hemodialysis kits and sets. According to the recall notice issued by Merit Medical Systems, Inc.' (Merit), in some cases the sheath introducer may not split as intended due to a design related issue. Published 2026-04-23.
What to do now
Contact the manufacturer if you require additional information.
Recall number
81915
Official notice
2026-04-23
The hazard
The hazard
Teleflex has initiated a voluntary recall for certain lots of the above-mentioned products due to receipt of a supplier-initiated recall of the Merit 16f dual-valved splittable sheath introducer component, which is included in impacted arrow hemodialysis kits and sets. According to the recall notice issued by Merit Medical Systems, Inc.' (Merit), in some cases the sheath introducer may not split as intended due to a design related issue.
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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Affected products
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Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Company & contacts
Company & contacts
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Brand: Arrow Subsidiary Of Teleflex.
Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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