Rifton Equipment recalled 3,238 TRAM powered lift devices on December 18, 2025, due to a risk of fraying body support straps. This recall affects models K310 sold worldwide, including the US, Europe, and Australia. Healthcare providers and patients must stop using the devices immediately to prevent injury.
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 Rifton TRAM is a powered lift device designed to assist in transferring clients in seated positions and aiding in sit-to-stand transfers and gait training. It is often used in healthcare settings to enhance patient mobility and safety during transfers.
The hazard arises from the potential fraying of the body support strap, which could compromise the device's ability to support clients properly. This failure during operation could lead to accidents and injuries.
This recall is not part of a broader industry pattern.
This recall affects the safety of patients and healthcare providers, necessitating immediate withdrawal of the devices from use to prevent possible injuries.
Serial numbers and ID codes are typically located on the device's control panel or near the base.
Expect a refund or replacement process to take about 4-6 weeks.
Keep records of your device's purchase details, including any receipts, warranty information, and correspondence with the manufacturer.
The recalled TRAM powered lift devices are identified by Model/Catalog Number: K310. The affected ID codes include K31020120704AA through K31020120718AB. The devices were distributed worldwide, including the US, Canada, and several countries in Europe and Asia.
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