# Major Recall Alert: Vectorflow Antegrade Catheterization Product Recalled Due to Sheath Introducer Issue from Teleflex
Teleflex has initiated a voluntary recall of certain lots of its **Vectorflow Antegrade Catheterization Product**, following a supplier-initiated recall by Merit Medical Systems, Inc. (Merit). The recall centers around a critical design flaw in the Merit 16f dual-valved splittable sheath introducer component. This component, which is included in impacted Arrow hemodialysis kits and sets, may fail to split as intended, posing potential safety risks during medical procedures.
## Why This Recall is Important
Medical devices like the Vectorflow Antegrade Catheterization Product play a pivotal role in patient care, specifically in hemodialysis treatments. Any malfunction in such devices could lead to critical delays or complications, compromising patient safety.
The design issue with the **Merit 16f dual-valved splittable sheath introducer** is particularly concerning since its failure to function as intended could lead to procedural interruptions. This underscores the importance of addressing the recall promptly to prevent further risks to healthcare providers and their patients.
## Details of the Recall
Here are the essential details about the Teleflex voluntary recall:
- **Affected Category**: Medical equipment (Vectorflow Antegrade Catheterization Product)
- **Issue**: Design flaw in Merit 16f dual-valved splittable sheath introducer, which may not split as expected during use
- **Impact**: The faulty component is included in impacted Arrow hemodialysis kits and sets
- **Reason for Recall Initiation**: Teleflex acted quickly after receiving a supplier-initiated recall notification from Merit due to the same design-related issue
- **Date of Recall Announcement**: [31986](https://recalls-rappels.canada.ca/en/alert-recall/vectorflow-antegrade-catheterization-product)
- **Image of Recalled Product**:
This recall reflects Teleflex's commitment to safety and transparency. Healthcare professionals and distributors are urged to check if they have affected lots of the product and take immediate action.
## What You Should Do
If you have purchased or are using the affected **Vectorflow Antegrade Catheterization Products**, here’s what you need to do:
- **Healthcare Facilities, Professionals, and Distributors**:
- Review your inventory for impacted product lots.
- Immediately stop using affected products.
- Follow the instructions provided by Teleflex on returning or replacing the recalled items.
- Contact Teleflex customer support for further guidance if needed.
- **Patients Using Affected Products**:
- Consult with your healthcare provider to determine if the recall affects any products you are currently using.
- Discuss potential alternatives or solutions with your medical team.
- **Report Issues**: If you encounter problems with a recalled product, report them promptly to Health Canada or through the company’s customer support channels.
For detailed information about this recall, visit the official notice on the **[Government of Canada recalls website](https://recalls-rappels.canada.ca/en/alert-recall/vectorflow-antegrade-catheterization-product)**.
## Stay Safe – Get Instant Recall Alerts
Recalls of medical devices like the Vectorflow Antegrade Catheterization Product highlight the critical importance of staying informed about product safety. Whether you’re a healthcare provider or concerned consumer, keeping updated can prevent potential hazards and save lives.
**Download the [MyRecalls App](#)** today to receive real-time alerts on product recalls in Canada. With our app, you can:
- Instantly track product recalls in your region
- Stay informed about recalls affecting your household or workplace
- Access key safety guidelines for impacted products
Being proactive about recalls is easy with MyRecalls – your one-stop resource for recall alerts that matter.
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Protecting patient safety and ensuring smooth healthcare operations starts with being informed. Take action today and stay ahead of critical medical product recalls!