# Major Recall Alert: Outer-Grip Locking Fem Implant Impactor Recalled Due to Manufacturing Error
On **March 7, 2025**, Smith & Nephew, Inc. initiated a critical recall for several lots of their **Outer-Grip Locking Fem Implant Impactor**. The recall stems from a **manufacturing error** that raises the risk of the **disassembly of the dowel pin and the impactor plate**, which could occur due to issues with the reaming of the drive shaft pin holes. This issue may compromise the reliability and safety of the affected lots, prompting the company to take swift action.
The recall has been listed under the **Health Canada alert system**, and consumers, medical professionals, and distributors are urged to take immediate measures to ensure public safety.
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## Why This Recall is Important
Recalls involving medical devices such as the Outer-Grip Locking Fem Implant Impactor are always significant because they directly impact patient health and safety. This implant impactor is a critical surgical tool used in orthopedic procedures. Any structural failure — including the **disassembly of the dowel pin and impactor plate** — during surgery could lead to delays, increased risks of complications, or harm to patients.
Smith & Nephew, Inc. has acted proactively by issuing this **voluntary recall** to address the potential risk of malfunction **before further incidents occur**. This underscores the critical importance of timely manufacturing and quality control inspections to minimize risks in the healthcare industry.
Consumers and medical centers should remain vigilant and refer to the impacted lot numbers to identify any recalled products immediately.
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## Details of the Recall
The recall applies specifically to certain lots of the **Outer-Grip Locking Fem Implant Impactor**, a medical device manufactured by **Smith & Nephew, Inc.**. Below are the key details:
- **Reason for Recall**: A manufacturing error that increases the risk of **dowel pin and impactor plate disassembly** due to improper reaming of the drive shaft pin holes.
- **Recall Start Date**: March 7, 2025
- **Products Affected**: Specific lots of the Outer-Grip Locking Fem Implant Impactor. Affected stakeholders are advised to refer to the official recall notice for a complete list of lot numbers.
- **Official Announcement**: [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/outer-grip-locking-fem-implant-impactor)
- **Image of the Affected Product**:
Smith & Nephew, Inc. is working closely with regulatory authorities to remove affected lots from distribution channels and ensure proper disposal of the recalled products.
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## What You Should Do
If your organization or medical practice uses the **Outer-Grip Locking Fem Implant Impactor**, here’s what you should do immediately:
- **Check Your Inventory**: Identify if you have a product from the affected lots.
- **Stop Use of Affected Products**: Cease using any identified recalled items to avoid potential safety risks.
- **Contact the Company**: Reach out to **Smith & Nephew, Inc.** or your local distributor for guidance on the return or replacement process.
- **Notify Stakeholders**: Inform all team members and relevant authorities to minimize the likelihood of use during surgical operations.
Prompt action can significantly reduce the risks associated with this recall.
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## Stay Safe – Get Instant Recall Alerts
Product recalls like this emphasize the importance of staying informed about safety issues in real time. Download the **[MyRecalls App](https://myrecalls.app)** to get **instant alerts** on the latest recalls for all categories, including medical devices, food, and electronics. With customized notifications and a user-friendly interface, you’ll never miss critical safety announcements again.
For full details on this recall, visit the [official recall notice here](https://recalls-rappels.canada.ca/en/alert-recall/outer-grip-locking-fem-implant-impactor).
Act now to stay informed and protect your patients. Stay safe, stay updated!