Public recall detail

Vectorflow Antegrade Catheterization Product

2026-04-23

medium
Gastroenterology and urology Performance
Quick summary

Quick summary: Vectorflow Antegrade Catheterization Product. Reason: Performance. Category: Gastroenterology and urology. Date: 2026-04-23.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Vectorflow Antegrade Catheterization Product. Reason: Performance. Category: Gastroenterology and urology. Date: 2026-04-23.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandArrow International Llc Subsidiary Of Teleflex Incorporated
ProductVectorflow Antegrade Catheterization Product
IssueMedical devices - Performance
Recall classType II
IdentificationRA-81915

Affected products

ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15232-VF *)
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15232-VFIM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15232-VFI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15232-VFM *)
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15552-VFI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15192-VFIM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15192-VFM *)
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15422-VFI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15192-VFI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15272-VF *)
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product
ProductVectorflow Antegrade Catheterization Product
LotMore than 10 numbers, contact manufacturer.
ModelCS-15312-VFI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVectorflow Antegrade Catheterization Product

Issue

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.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - Gastroenterology and urology
CompaniesArrow International Llc Subsidiary Of Teleflex Incorporated 3015 Carrington Mill Blvd., Morrisville, North Carolina, United States, 27560
Recall date2026-04-14
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81915
Background{}
CompaniesArrow International Llc Subsidiary Of Teleflex Incorporated 3015 Carrington Mill Blvd., Morrisville, North Carolina, United States, 27560
AudiencesGeneral public Healthcare Industry
Source updated2026-04-23

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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