Changeflow GovPing Healthcare & Life Sciences Teleflex Recalls Vectorflow Catheter Products
Urgent Enforcement Amended Final

Teleflex Recalls Vectorflow Catheter Products

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Summary

Arrow International LLC, a subsidiary of Teleflex Incorporated, has initiated a voluntary recall for certain lots of Vectorflow Antegrade Catheterization Products (11 model numbers including CS-15232-VF, CS-15232-VFIM, CS-15232-VFI, CS-15232-VFM, CS-15552-VFI, CS-15192-VFIM, CS-15192-VFM, CS-15422-VFI, CS-15192-VFI, CS-15272-VF, and CS-15312-VFI). The recall was triggered by a supplier-initiated recall of the Merit 16f dual-valved splittable sheath introducer component, included in impacted Arrow hemodialysis kits and sets, due to reports that the sheath introducer may not split as intended due to a design-related issue. Health Canada classified this as a Type II recall on April 14, 2026, under identification number RA-81915.

“in some cases the sheath introducer may not split as intended due to a design related issue.”

Published by Health Canada on recalls-rappels.canada.ca . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

About this source

Health Canada operates a single recalls and safety alerts portal covering food, drugs, medical devices, consumer products, vehicles, and cosmetics. Roughly 100 alerts a month, with each entry tagged by hazard type, affected lots, distributor, and recommended consumer action. The portal is bilingual and aligns closely with FDA recalls in scope, so a Health Canada alert often signals a US recall is coming or has just landed. Watch this if you sell into Canada, run cross-border product compliance, or trade pharma equities exposed to recall events. Recent examples: Stryker Variax 2 locking screws pulled non-sterile, a Baxter head positioning adapter Type I recall, an Alecensaro hypertriglyceridemia and pancreatitis safety signal.

What changed

Health Canada issued a Type II medical device recall for Vectorflow Antegrade Catheterization Products manufactured by Arrow International LLC (a subsidiary of Teleflex Incorporated). The recall affects 11 product model numbers and was triggered by a supplier-initiated recall from Merit Medical Systems, Inc. regarding the Merit 16f dual-valved splittable sheath introducer component, which may fail to split as intended due to a design-related issue.

Healthcare facilities and catheterization labs that use these products should verify whether they have any affected lots in stock and contact the manufacturer directly for return or replacement instructions. The lot numbers span more than 10 batches, and facilities should obtain specific lot information by contacting Arrow International LLC at their Morrisville, North Carolina address.

What to do next

  1. Contact the manufacturer if you require additional information.

Archived snapshot

Apr 24, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Health product recall

Vectorflow Antegrade Catheterization Product

Brand(s)

Arrow International Llc Subsidiary Of Teleflex Incorporated

Last updated

2026-04-23

Summary

Product Vectorflow Antegrade Catheterization Product Issue Medical devices - Performance What to do Contact the manufacturer if you require additional information.

Affected products

Affected products Lot or serial number Model or catalogue number
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15232-VF *)
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15232-VFIM
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15232-VFI
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15232-VFM *)
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15552-VFI
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15192-VFIM
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15192-VFM *)
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15422-VFI
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15192-VFI
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15272-VF *)
Vectorflow Antegrade Catheterization Product More than 10 numbers, contact manufacturer. CS-15312-VFI

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.

Additional information

Details

Original published date:

2026-04-23

Alert / recall type Health product recall Category Health products - Medical devices - Gastroenterology and urology Companies Arrow International Llc Subsidiary Of Teleflex Incorporated

3015 Carrington Mill Blvd., Morrisville, North Carolina, United States, 27560

Published by Health Canada Audience General public Healthcare Industry Recall class Type II Recall date

2026-04-14

Identification number RA-81915

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Last updated

Classification

Agency
Health Canada
Filed
April 23rd, 2026
Instrument
Enforcement
Branch
Executive
Legal weight
Binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Healthcare providers Manufacturers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Product recall response
Geographic scope
Canada CA

Taxonomy

Primary area
Medical Devices
Operational domain
Clinical Operations
Compliance frameworks
GxP
Topics
Product Safety Healthcare

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