# Major Recall Alert: System 8 Reciprocating Saw, System 9 Reciprocating Saw, and System 9 Sternum Saw Recalled Due to Blade Retention Failure Risk
On **March 14, 2025**, a critical recall was issued for the **System 8 Reciprocating Saw, System 9 Reciprocating Saw**, and **System 9 Sternum Saw**. The recall addresses a serious safety concern regarding the product's internal compression spring (part number 0038-419-000). This spring has the potential to disengage during blade loading and unloading. If disengaged, this defect could result in **blade retention failure**, posing significant safety risks for operators.
If you or your organization utilize any of these saws, **this recall demands your immediate attention.**
## Why This Recall is Important
The recalled saws are commonly used in medical and surgical environments, where proper function is critical for both patient safety and procedural efficiency. This recall was initiated because the **compression spring may disengage** within the saw's drivetrain assembly.
When this occurs:
- The **blade collar fails to spring back** to its original position.
- There is a heightened risk of **blade retention failure** during blade replacement or usage.
- This malfunction could lead to **operational delays or hazards** in surgical environments.
Such a defect is unacceptable in high-stakes environments, reinforcing the need for medical professionals and institutions to act promptly on this recall.
## Details of the Recall
The recall specifically applies to the following products under the **System 8 and System 9** brands by Stryker Instruments:
- **System 8 Reciprocating Saw**
- **System 9 Reciprocating Saw**
- **System 9 Sternum Saw**
### Recall Summary:
- **Recall Reason:** Potential disengagement of the **compression spring (0038-419-000)** inside the drivetrain assembly.
- **Impact:** Blade retention failure during loading or unloading.
- **Recall Start Date:** March 14, 2025
- **Source:** [Government of Canada Official Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/stryker-instruments-system-8-and-9-saws)
If you own or operate one of these tools, stop use immediately and follow the steps outlined below.
## What You Should Do
To address this issue and ensure workplace or procedural safety, take the following actions:
- **Identify Affected Products:** Check the make and model of your reciprocating or sternum saw to confirm if it matches the recalled models.
- **Contact the Manufacturer:** Reach out to Stryker Instruments to learn about replacement parts, repairs, or refunds.
- **Halt Usage Immediately:** Do not continue to use defective saws, as this may pose risks to personnel and patients.
- **Share the Information:** Inform your team members, supervisors, or departments managing surgical equipment to ensure widespread awareness of this critical recall.
Taking these steps promptly will ensure that you remain compliant and safeguard against potential errors during medical procedures.
## Stay Safe – Get Instant Recall Alerts
Staying informed about recalls is essential, particularly in industries where product functionality directly affects safety and lives. To avoid missing vital updates like this one:
- **Download the MyRecalls App** today! This free app keeps you informed about the latest recalls in Canada. Receive instant alerts for **medical equipment, consumer goods, and more.**
- [Click here to download now!](https://myrecalls.app)
For a more detailed overview of this recall, visit the [official Canada recall page](https://recalls-rappels.canada.ca/en/alert-recall/stryker-instruments-system-8-and-9-saws).
### Final Word
Product recalls like this emphasize the importance of robust safety protocols to protect users and patients alike. Stay informed, act quickly, and don’t take risks with defective equipment. Follow the recall instructions for the **System 8 Reciprocating Saw**, **System 9 Reciprocating Saw**, and **System 9 Sternum Saw** to maintain a safe working environment.
Stay safe—**don’t risk it, check it!**