Rifton Equipment recalled 1,096 units of the Low Base TRAM on December 18, 2025, due to a potential fraying hazard on the body support strap. The recall affects models distributed worldwide, including the US, Canada, and several countries in Europe and Asia. Patients and healthcare providers are advised to stop using this 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 Low Base TRAM is a powered lift device designed to assist in transferring clients in a seated position and helping with sit-to-stand transfers. It is commonly used in healthcare settings for patients with mobility challenges.
The body support strap may fray, which could compromise the device's ability to safely support patients during transfers. If the strap fails, it can lead to serious injuries from falls.
This recall is not part of a broader industry pattern.
The recall affects a significant number of devices used in healthcare, creating urgency for immediate action to prevent potential injuries.
The model number and ID codes can typically be found on a label attached to the device's frame or on the user manual.
Expect a refund or replacement process to take approximately 4-6 weeks after contacting the manufacturer.
Keep all receipts, correspondence with the manufacturer, and photos of the product as documentation for your records.
The recalled product is the Low Base TRAM, Model/Catalog Number K320, with ID Codes ranging from K32020130515AA to K32020130812AB. The device is designed for transferring clients in a seated position and assisting in sit-to-stand transfers. It has been distributed worldwide, including in the US, UAE, Australia, Canada, EU, and others.
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