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Angiography Pack, Catheterization Packs Recall Due to Cardinal Health™ was re...

# Major Recall Alert: Angiography Pack, Catheterization Packs Recalled Due to Rotating Adaptor Safety Issue

Cardinal Health™ recently issued a vital notification to healthcare professionals and users regarding a medical device recall. Medline Industries has recalled certain Convenience Kits containing Namic Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA Syringes). These syringes are used in Angiography and Catheterization Packs, and the recall highlights a major safety concern: the potential for the rotating adaptor to unwind during use, leading to possible disconnection. In critical medical scenarios, this issue could pose serious risks to patient safety.

## Why This Recall is Important

Medical devices, particularly those intended for precise procedures such as angiography and catheterizations, play a pivotal role in ensuring successful medical outcomes. A defect like the one identified in the Namic RA Syringes can disrupt procedures, potentially causing harm to patients.

The Namic RA Syringes, known for their rotating adaptor mechanism, are an integral component of Medline Convenience Kits. These kits are widely distributed, making it essential for healthcare providers to act quickly to mitigate risks. If disconnection occurs during use, it may complicate treatment, delay procedures, or create critical safety issues. By identifying and addressing the problem promptly, healthcare providers can keep their patients safe while ensuring uninterrupted treatment.

## Details of the Recall

Key information regarding the recall includes:
- **Category of Products**: Medical device kits used in angiography and catheterization procedures.
- **Affected Products**: Angiography Pack, Catheterization Packs containing Namic RA Syringes.
- **Reason for Recall**: The rotating adaptor in these syringes may unwind during use, potentially resulting in disconnection.
- **Brand Involved**: Cardinal Health™ was informed of the recall, originating from Medline Industries’ Convenience Kits.
- **Date Announced**: The recall was announced to healthcare providers and stakeholders on March 19, 2013.
- **Product Concern**: The defect may interrupt critical medical procedures, posing a risk to patient safety.

For additional details, view the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/cardinal-healthtm-angiography-pack-and-catheterization-packs).

## What You Should Do

If your facility has received any Angiography or Catheterization Packs containing the Namic RA Syringes, it is essential to take immediate action:

- **Stop Using the Affected Kits**: Discontinue use of these packs to avoid potentially hazardous situations during medical procedures.
- **Review Inventory**: Check your supplies to identify whether your kits include the recalled syringes.
- **Contact Manufacturer**: Reach out to Medline Industries or Cardinal Health™ for guidance on how to return or replace affected products.
- **Alert Your Team**: Inform all staff at your medical facility about the recall and advise them to follow updated protocols.
- **Report Adverse Events**: If you’ve experienced issues with the product, report incidents to the appropriate regulatory authority in your region.

Addressing the recall proactively can ensure patient safety and regulatory compliance within your practice or healthcare facility.

## Stay Safe – Get Instant Recall Alerts

Medical equipment recalls can arise without warning, making it crucial to stay informed about potential risks to patient safety. Don’t miss critical updates like this one! Download the **Recall App** today to receive real-time alerts about recalls affecting medical devices, consumer goods, and more.

Stay one step ahead of safety concerns by ensuring your devices meet the current standards. Visit the [official recall source](https://recalls-rappels.canada.ca/en/alert-recall/cardinal-healthtm-angiography-pack-and-catheterization-packs) for more information.

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**Your patients’ safety is your top priority. Take action today to address this critical recall and ensure your facility continues to operate safely without interruptions.**

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