# Major Recall Alert: Thunderbeat Type S Hand Instruments, Thunderbeat, Front-Actuated Grip, Thunderbeat, Inline Grip, Thunderbeat, Pistol Grip Recalled
Olympus has issued a critical product removal action for its unexpired **Thunderbeat Hand Instruments**, including the **Thunderbeat Type S Hand Instruments**, **Thunderbeat Front-Actuated Grip**, **Thunderbeat Inline Grip**, and **Thunderbeat Pistol Grip**. This urgent recall requires all users to immediately stop using these devices, quarantine the affected products, and contact Olympus’s customer service to obtain an RMA for safe product returns.
This situation raises significant safety concerns, impacting healthcare providers worldwide. If you or your facility utilizes these instruments, read on for full details, important next steps, and how to stay up-to-date with vital recall information.
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## Why This Recall Is Important
The recall was announced on **October 31, 2023**, and applies to all unexpired **Thunderbeat Hand Instruments** produced by Olympus. These devices are critical components in healthcare settings, often used in surgeries and other medical procedures. Yet, an identified safety concern has prompted Olympus to take proactive action to safeguard users and patients.
Failing to adhere to the recall instructions may pose potential risks to patient safety and interfere with surgical outcomes, signaling the utmost importance for all users to act immediately. Healthcare facilities and professionals are urged to follow Olympus’s guidance to prevent any potential harm.
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## Details of the Recall
Here’s what you need to know about the Olympus Thunderbeat Hand Instruments recall:
- **Category**: Medical Device Recall (CAN)
- **Products Affected**:
- **Thunderbeat Type S Hand Instruments**
- **Thunderbeat Front-Actuated Grip**
- **Thunderbeat Inline Grip**
- **Thunderbeat Pistol Grip**
- **Reason for Recall**: Olympus has issued this product removal action for *unexpired* Thunderbeat instruments to address a potential safety risk. Users are required to quarantine and return all affected devices for corrective action.
- **Announced Date**: October 31, 2023
- **Action Required**:
- Cease immediate use of all impacted Thunderbeat hand instruments.
- Quarantine the affected items.
- Contact Olympus Customer Service to acquire a **Return Merchandise Authorization (RMA)** form for product returns.
For more information, visit the **official recall notice** here: [Olympus Thunderbeat Hand Instruments Recall](https://recalls-rappels.canada.ca/en/alert-recall/thunderbeat-hand-instruments).
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## What You Should Do
### Follow These Steps to Act on the Recall Immediately:
1. **Stop Usage**: Immediately cease using all unexpired Thunderbeat Hand Instruments.
2. **Quarantine Devices**: Separate the affected instruments from other medical devices to prevent unintended use.
3. **Contact Olympus Customer Service**: Request an RMA form and follow the provided instructions for returning the products safely.
4. **Spread Awareness**: Notify other medical personnel and facilities within your network to ensure a coordinated response.
The recall emphasizes the importance of swift action to protect patients, practitioners, and healthcare operations.
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Ensuring medical devices are safe for use is paramount, and Olympus’s proactive recall of the Thunderbeat Hand Instruments underscores the need for diligence in protecting healthcare workers and patients. Share this information with your colleagues, download the Recall Alerts App, and make health and safety your top priority.
For further details on this recall, check out the official announcement here: [Thunderbeat Hand Instruments Recall](https://recalls-rappels.canada.ca/en/alert-recall/thunderbeat-hand-instruments).