Recall Z-1137-2026— Community Products, LLC

Class II · Ongoing

Class II FDA medical device recall by Community Products, LLC, initiated 2025-12-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.. Reason: Potential for fraying on the body support strap..

Recalling firm
Community Products, LLC
Classification
Class II
Status
Ongoing
Initiated
2025-12-18
Firm location
Rifton, NY, United States

Product description

Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.

Reason for recall

Potential for fraying on the body support strap.

Data sourced from openFDA. This site is unofficial and independent of the FDA.