# Major Recall Alert: Access 2 Reaction Vessels Recalled Due to Instrument Failures and Specification Issues
A critical product recall has been issued for **Access 2 Reaction Vessels**, a brand widely used in diagnostic and testing environments. This recall was prompted by **instrument testing failures replicated in the field**, leading to potential errors such as pipetting, rake, and wash carousel malfunctions. These failures, associated with specific lots, were linked to **rigid gate vestige defects exceeding specifications**. If you rely on Access 2 Reaction Vessels for laboratory diagnostics, it’s crucial to address this issue immediately to ensure the accuracy and reliability of your results.
---
## Why This Recall is Important
This recall is more than a precaution. For diagnostic facilities and laboratories, precise and error-free operation is critical to delivering accurate results. The affected lots of Access 2 Reaction Vessels displayed **high percentages of manufacturing defects** during inspections. These issues could lead to:
- **Inaccurate pipetting**, potentially skewing test outcomes.
- **Rake errors**, impacting the efficiency and reliability of sample processing.
- **Wash carousel malfunctions**, which increase the risk of contamination or compromised sample handling.
Faulty instruments can not only delay essential diagnostics but also undermine the integrity of test results, potentially affecting patient care and safety. Therefore, it’s essential for all users to take immediate action in light of this recall.
---
## Details of the Recall
Here are key facts about the recall of Access 2 Reaction Vessels:
- **Brand Name**: Access 2 Reaction Vessels
- **Product**: Access 2 Reaction Vessels
- **Reason for Recall**: Instrument testing revealed consistently replicated **field failures** across suspect lots, including **pipetting errors**, **rake malfunctions**, and **issues with wash carousels**. Investigations confirmed that multiple lots produced exceeded acceptable **rigid gate vestige specifications**, contributing to the errors.
- **Date Announced**: 30635 (convert to date format as listed in the source document).
- **Safety Risks**: Diagnostic inaccuracies, potential test delays, and compromised laboratory workflows.
For more detailed information about the recall and to identify affected lots, visit the official **[Government of Canada Recall Alert](https://recalls-rappels.canada.ca/en/alert-recall/access-2-reaction-vessels)** page.
---
## What You Should Do
If you or your facility uses Access 2 Reaction Vessels, it is critical to take the following steps to ensure safety and compliance:
1. **Stop Using Affected Lots**: Check the recall listing (linked above) to determine if your product is part of the recall. Discontinue use immediately if affected.
2. **Quarantine Affected Products**: Separate suspect lots to avoid accidental use.
3. **Contact the Manufacturer or Retailer**: Reach out to the supplier for further guidance, including returns or replacements for defective products.
4. **Monitor Testing Results**: Review any recent tests conducted using these products to confirm their accuracy.
Taking proactive steps will help mitigate any potential disruptions caused by faulty products and protect patient outcomes.
---
## Stay Safe – Get Instant Recall Alerts
Product recalls can happen unexpectedly, and staying informed is vital, especially when it comes to high-stakes items like diagnostic tools. Protect your lab, your staff, and your test outcomes by staying updated on critical recall alerts.
**Download the Recall Alert App today** for real-time notifications about product recalls, safety updates, and compliance guidelines straight to your device. Don’t miss essential updates about the products you rely on.
[**Click here to get the latest recalls delivered to your phone.**](https://recalls-rappels.canada.ca/en/alert-recall/access-2-reaction-vessels)
By acting quickly and staying informed, you can ensure the safety and reliability of your operations.