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.