Community Products Recalls

3 recalls found for Community Products. Check if any of your products are affected.

HIGHFDA DEVICE

Rifton Equipment Recalls Low Base TRAM Due to Fraying Hazard

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.

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HIGHFDA DEVICE

Rifton Equipment Recalls TRAM Lift Device Over Strap Hazards

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.

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Brand Statistics

Total Recalls
3
Pages
1