# Major Recall Alert: Heyman Follower Recalled Due to Incorrect French Size Labeling
Medical professionals and healthcare providers across Canada, take note: a major recall involving the **Heyman™ straight and coude followers** has been issued due to a labeling error. The recall, initiated by BD as part of its quality assurance protocols, was officially announced on **June 3, 2025**. The issue? An incorrect French size has been printed on the product, posing serious risks for clinical use. Here's what you need to know.
## Why This Recall is Important
The **Heyman™ Follower**, a widely used medical device, is essential for various healthcare procedures that require precise sizing. However, the discovery of **incorrectly labeled French sizes** could lead to serious complications, including incorrect procedures, patient discomfort, or more severe medical outcomes. Medical devices must meet strict labeling protocols to ensure safety and effectiveness, and this error highlights the importance of proactive product monitoring and swift action.
This recall serves as a reminder of the potential risks associated with mislabeling and the critical role accuracy plays in healthcare environments. If left unaddressed, such discrepancies could compromise patient care and treatment outcomes.
## Details of the Recall
BD's internal investigation identified the issue and prompted the company to act responsibly, notifying healthcare providers and recalling affected products. Below are the recall details:
- **Category**: Medical Device Recall – Canada
- **Product Name**: Heyman™ Straight and Coude Followers
- **Brand**: Heyman™ Follower
- **Recall Start Date**: June 3, 2025
- **Issue**: Incorrect French size printed on the product label, leading to potential misuse in clinical settings.
- **Safety Measures**:
- Immediate product retrieval
- Notification to all affected healthcare providers
- Replacement or correction of mislabeled products
It is critical for all healthcare institutions and medical professionals to review their inventory for potentially affected Heyman™ Followers, prevent usage, and follow recall instructions issued by BD.
For the full recall notice, visit the official Government of Canada recall page [here](https://recalls-rappels.canada.ca/en/alert-recall/heyman-follower).
## What You Should Do
If your facility uses Heyman™ Followers, here’s what you need to do immediately:
- **Inspect Your Inventory**: Check all Heyman™ straight and coude followers for the recall notice.
- **Cease Usage**: Discontinue the use of affected products immediately to prevent any incidents.
- **Follow Instructions**: Reach out to BD for guidance on returning or replacing mislabeled products.
- **Notify Staff**: Inform all relevant healthcare workers in your organization about the recall to ensure proper compliance and patient safety.
BD is committed to resolving this issue efficiently. If you have any concerns, contact the product manufacturer or your medical supplier for detailed instructions.
## Stay Safe – Get Instant Recall Alerts
Medical equipment recalls are time-sensitive and can directly impact patient care. Don't miss critical updates – stay informed with the latest recall alerts by downloading **[Canada's recall app](https://recalls-rappels.canada.ca/en/alert-recall/heyman-follower)**. With real-time notifications and comprehensive recall information at your fingertips, you can ensure your practice remains safe and compliant.
Protecting patient safety starts with staying informed. Act now, review your inventory, and take preventive measures to eliminate risks. For more information, visit the official **[Heyman™ Follower recall page](https://recalls-rappels.canada.ca/en/alert-recall/heyman-follower)** today.
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