Community Products, LLC recalls Rifton Equipment
- Recalling company
- Community Products, LLC
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Dec 18, 2025
- Reported
- Jan 28, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.
- Status
- Ongoing
- Quantity
- 1,096 units
- Lot / codes
- Model/Catalog Number: K320. ID Codes: K32020130515AA, K32020130603AA, K32020130606AA, K32020130607AB, K32020130610AA, K32020130612AA, K32020130617AA, K32020130617AB, K32020130618AA, K32020130709AA, K32020130713AA, K32020130713AB, K32020130717AB, K32020130802AA, K32020130805AA, K32020130807AA, K32020130808AA, K32020130808AB, K32020130812AA, K32020130812AB, K32020130812AC, K32020130812AD, K32020130813AA, K32020130814AA, K32020130820AA, K32020130822AA, K32020130823AA, K32020130824AA, K32020130827AA, K32020130827AB, K32020130828AA, K32020130830AA, K32020130907AA, K32020130909AB, K32020130909AC, K32020130909AD, K32020130909AE, K32020130919AA, K32020130920AA, K32020130924AA, K32020131007AA, K32020131007AB, K32020131009AA, K32020131017AB, K32020131021AA, K32020131022AB, K32020131022AC, K32020131022AD, K32020131024AA, K32020131025AA, K32020131029AA, K32020131031AA, K32020131101AA, K32020131102AA, K32020131107AA, K32020131115AD, K32020131119AA, K32020131120AD, K32020131205AA, K32020131210AA, K32020131217AD, K32020140103AA, K32020140113AA, K32020140115AA, K32020140117AA, K32020140121AA, K32020140122AA, K32020140122AB, K32020140125AA, K32020140130AB, K32020140210AA, K32020140218AA, K32020140218AB, K32020140220AA, K32020140221AA, K32020140224AA, K32020140304AA, K32020140305AB, K32020140312AA, K32020140315AA, K32020140327AA, K32020140327AC, K32020140401AA, K32020140407AA, K32020140407AB, K32020140408AA, K32020140412AA, K32020140415AA, K32020140417AA, K32020140422AA, K32020140423AA, K32020
- Company location
- Rifton, NY
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1138-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1138-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.