FDA DevicesClass II
Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a po...
Published: January 28, 2026Recall ID: Z-1138-2026Category: devicesCountry: US
Reason for Recall / Hazard
Potential for fraying on the body support strap.
Product Description & Identification
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.
Affected Products
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.
Additional Source Details
| Field | Value |
|---|---|
| City | Rifton |
| State | NY |
| Event id | 98140 |
| Address 1 | 2032 Route 213 |
| Code info | 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, K3... [TRUNCATED] |
| Postal code | 12471 |
| Report date | 20260128 |
| Product type | Devices |
| Product quantity | 1,096 units |
| Reason for recall | Potential for fraying on the body support strap. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251218 |
| Initial firm notification | |
| Center classification date | 20260122 |
Overview
- Recalling FirmCommunity Products, LLC
- StatusOngoing
- Risk LevelClass II
- DistributionWorldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.