Community Products recalls Rifton Equipment Low Base TRAM model K320 due to potential fraying on the body support strap. This powered lift device is used for transferring clients in seated positions or sit-to-stand transfers. Affected units have specific model IDs listed in the recall notice.
Potential for fraying on the body support strap.
Community Products is recalling Rifton Equipment Low Base TRAM models K320 because the body support strap may fray. This could lead to the user being unable to safely transfer clients during seated or sit-to-stand movements. The recall affects specific model numbers with unique ID codes.
The body support strap in these units may fray over time, which could cause the user to lose control during client transfers. This risk is highest when moving clients from seated to standing positions or assisting with gait training.
People who own or use Rifton Equipment Low Base TRAM models K320 for client transfers are affected. Those using the device for sit-to-stand transfers or seated transfers are most at risk due to potential strap fraying.
Check if your Rifton Equipment Low Base TRAM has model number K320 and ID codes listed in the recall notice. The product is used for transferring clients in seated positions or sit-to-stand transfers and gait training.
Inspect the body support strap for signs of fraying or damage.
Reach out to Community Products for guidance on next steps.
The recall notice states this is a powered lift device for transferring clients in seated positions or assisting in sit-to-stand transfers and gait training, so it's used in professional healthcare settings.
Check if your Rifton Equipment Low Base TRAM has model number K320 and one of the specific ID codes listed in the recall notice.
The recall notice does not specify a fix for fraying straps; you should contact Community Products for guidance.
We’ve drafted a message you can send Community Products to request your refund or repair — edit it as you like.
Subject: Recall Z-1138-2026 — Community Products Community Products Hello, I own a Community Products that is covered by recall Z-1138-2026 from Community Products. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
