Rifton Equipment recalled 470 E-Pacer gait training devices on December 18, 2025. The body support strap may fray, posing a risk to users. Health care providers and patients must stop using the device immediately.
Potential for fraying on the body support strap.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Community Products, LLC or your healthcare provider for instructions. Notification method: E-Mail
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The E-Pacer is a gait training device designed to assist individuals in transitioning from sitting to standing. It is commonly used in rehabilitation settings for patients with mobility issues.
The device's body support strap may fray, potentially causing it to fail during use. This could lead to falls or other injuries during rehabilitation exercises.
This recall is not part of a broader industry pattern.
Consumers may experience significant inconvenience as they must cease use of the E-Pacer and seek alternative mobility aids while waiting for further instructions.
The model number and ID codes are typically found on the device's label or near the power height adjustment mechanism.
Expect a response regarding refund or replacement within 4-6 weeks after contacting Community Products.
Keep copies of any emails, receipts, and correspondence related to the recall for your records.
The recalled E-Pacer is identified by Model/Catalog Number: K660. It was distributed worldwide, including the US, Canada, Australia, and several other countries. The affected units were sold under the Community Products brand.
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