Recall Z-1138-2026— Community Products, LLC

Name: FDA recall Z-1138-2026
Creator: U.S. Food and Drug Administration
Published: 2025-12-18

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, Low Base TRAM. Model/Catalog Number: K320. 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. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds.. 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, Low Base TRAM. Model/Catalog Number: K320. 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. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds.

Reason for recall

Potential for fraying on the body support strap.

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