Community Products, LLC

FDA Regulatory Profile

Summary

Total Recalls
6
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1137-2026Class IIRifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transfeDecember 18, 2025
Z-1138-2026Class IIRifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device foDecember 18, 2025
Z-1139-2026Class IIRifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device witDecember 18, 2025
Z-0164-2020Class IIRifton TRAM Standard Base, SKU K310, powered lift deviceMarch 21, 2019
Z-0165-2020Class IIRifton TRAM Low Base, SKU K320, powered lift deviceMarch 21, 2019
Z-0166-2020Class IIRifton E-Pacer, SKU K660, powered lift deviceMarch 21, 2019