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Broviac 6.6 Fr Single-Lumen CV Catheter Peel-Apart Introducer Kit With SureCu...

# Major Recall Alert: Broviac and Hickman Central Venous Catheter Kits Recalled Due to Potential Packaging Damage Impacting Sterility

**Attention healthcare providers and patients:** A significant recall has been issued for Broviac and Hickman central venous catheter kits due to concerns about potential packaging damage that may compromise the sterile barrier. Manufactured by BD, these products are critical for use in medical settings, which makes this recall especially urgent. Keep reading for important details about the affected products and steps you should take if you have these kits in your possession.

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## Why This Recall is Important

Patient safety is a top priority in healthcare, and the sterility of medical devices plays a crucial role in preventing infections. BD discovered, during internal inspections, that some of its Hickman and Broviac catheter kits may have damaged outer tray packaging. This issue could compromise the sterility of the inner tray surface and the included instructions for use, creating a potential risk for infection.

As these catheter kits are commonly used in central venous access procedures, the possibility of contamination poses a serious risk to patients. Sterile barriers ensure safe device handling, and any compromise in packaging integrity can lead to considerable health consequences, especially for immunocompromised individuals.

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## Details of the Recall

The recall covers the following catheter kits:

- Broviac™ 6.6 Fr Single-Lumen CV Catheter Peel-Apart Introducer Kit With SureCuff™ Tissue Ingrowth Cuff
- Hickman™ 12.5 Fr Triple-Lumen CV Catheter Peel-Apart Introducer Kit With SureCuff™ Tissue Ingrowth Cuff
- Hickman™ 9.6 Fr Single-Lumen CV Catheter Peel-Apart Introducer Kit With SureCuff™ Tissue Ingrowth Cuff
- Hickman™ Dual-Lumen CV Catheter With SureCuff™ Tissue Ingrowth Cuff

### Reason for Recall
BD’s quality inspections identified damage to the outer tray packaging of these kits. The packaging has a double-tray structure—comprising an outer tray and an inner tray. Although the catheter and accessories remain sealed within the inner tray, damage to the outer tray could compromise the infectious safety of:

- The **outer surface of the inner tray**
- The **instructions for use enclosed in the packaging**

This contamination risk stems from the potential for compromised sterility, which could have serious implications in clinical procedures.

For full recall details, visit the official source: [Hickman™ and Broviac™ Central Venous Catheter Kits Recall](https://recalls-rappels.canada.ca/en/alert-recall/hickmantm-and-broviactm-central-venous-catheter-kits).

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## What You Should Do

If you possess any of the affected Hickman or Broviac catheter kits, follow these steps immediately:

1. **Stop using the recalled products**: Ensure that any impacted kits are identified and removed from use in healthcare facilities.
2. **Follow recall instructions**: Contact BD for further guidance on returning or replacing the products, as outlined in the recall notice.
3. **Notify healthcare providers and patients**: Healthcare institutions should inform relevant personnel and patients about the recall to mitigate any risks.
4. **Report any adverse incidents**: For Canada-based cases, report issues via Health Canada's [MedEffect Program](https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada.html).

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## Stay Safe – Get Instant Recall Alerts

Staying informed about product recalls is critical for both patient safety and compliance with healthcare standards. Avoid missing important updates by downloading a dedicated recall alert app today. Get real-time notifications for medical equipment, pharmaceuticals, and other products that impact health and safety.

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**Ensure patient safety and reduce risks by acting immediately on recall notices. For the latest updates and further details, visit the official recall page here: [Hickman™ and Broviac™ Central Venous Catheter Kits Recall](https://recalls-rappels.canada.ca/en/alert-recall/hickmantm-and-broviactm-central-venous-catheter-kits).**

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