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Community Products Recalls
6 recalls on record · October 30, 2019 to January 28, 2026 · Medical Devices
Recalls by year
19
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 28, 2026Medical DevicesFDA
Community Products, LLC recalls Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjus
Hazard: Potential for fraying on the body support strap.
January 28, 2026Medical DevicesFDA
Community Products, LLC recalls Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clien
Hazard: Potential for fraying on the body support strap.
January 28, 2026Medical DevicesFDA
Community Products, LLC recalls Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a s
Hazard: Potential for fraying on the body support strap.
October 30, 2019Medical DevicesFDA
Community Products, LLC recalls Rifton E-Pacer, SKU K660, powered lift device
Hazard: A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
October 30, 2019Medical DevicesFDA
Community Products, LLC recalls Rifton TRAM Low Base, SKU K320, powered lift device
Hazard: A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
October 30, 2019Medical DevicesFDA
Community Products, LLC recalls Rifton TRAM Standard Base, SKU K310, powered lift device
Hazard: A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.