# Major Recall Alert: BD BACTEC™ MGIT™ 960 PZA Kit Recalled Due to Modified Version of Kit and Reduced Shelf-Life
BD (Becton, Dickinson, and Company) has announced a significant update regarding the BD BACTEC™ MGIT™ 960 PZA Kit used in clinical laboratory testing. This recall follows previous field safety notifications (IDS-24-5091/IDS-25-5091-EXP) to address safety and performance concerns. The company has resumed production of a modified version of the kit, which includes changes to inoculation methods and a reduced shelf-life. Here’s what you need to know about this recall and how it impacts you.
## Why This Recall is Important
The BD BACTEC™ MGIT™ 960 PZA Kit plays a critical role in testing for tuberculosis and related conditions. Healthcare providers and laboratories rely on the accuracy and reliability of this kit to make important diagnostic decisions. Any irregularities or safety issues could significantly impact patient outcomes. By issuing this follow-up notification, BD aims to ensure the safe use of their product with updated guidance on the following:
- **Modified inoculation methods**: Changes to the way the kit should be used.
- **Reduced shelf-life**: Updated expiration dates to maintain product integrity.
- **Customer communications**: Ensuring all users are informed of the updates for proper implementation.
BD’s commitment to patient safety and quality control underpins this recall notification, ensuring customers adhere to the updated instructions to avoid any testing inaccuracies.
## Details of the Recall
Here are the key details of the recall for quick reference:
- **Category**: Canada (follow-up to field safety notifications IDS-24-5091/IDS-25-5091-EXP)
- **Product Name**: BD BACTEC™ MGIT™ 960 PZA Kit
- **Reason for Recall**: Notification of a modified version of the product, including changes to inoculation procedures and revised shelf-life.
- **Safety Measures**: Follow updated guidance provided by BD to ensure proper use of the kit.
- **Date Announced**: Official announcement on recall monitoring available [here](https://recalls-rappels.canada.ca/en/alert-recall/bd-bactectm-mgittm-960-pza-kit).
Laboratories and healthcare providers using this kit are strongly advised to review the safety notification and the updated instructions to avoid any issues related to the revised product specifications.
## What You Should Do
If you are a clinician, lab technician, or healthcare provider currently using or stocking the BD BACTEC™ MGIT™ 960 PZA Kit, here’s what you should do immediately:
- **Review Field Safety Notifications**: Ensure you have read IDS-24-5091/IDS-25-5091-EXP to understand all necessary changes.
- **Update Procedures**: Implement updated inoculation methods as outlined in BD’s communication.
- **Check Expiration Dates**: Identify kits with the reduced shelf-life and ensure prompt usage or safe disposal.
- **Contact BD for Questions**: If you have concerns or need additional support, reach out to BD’s customer service team for clarification.
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For more information on this recall, visit the official Government of Canada recall page [here](https://recalls-rappels.canada.ca/en/alert-recall/bd-bactectm-mgittm-960-pza-kit).
Take action today! Stay informed – stay safe.