Community Products recalls Rifton TRAM Standard Base (SKU K310) due to design change in load-bearing buckle causing spring fatigue failure after repeated use. Affected units have specific ID codes listed in the recall.
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Community Products is recalling their Rifton TRAM Standard Base powered lift devices (SKU K310) because a design change in the load-bearing quick release buckle can cause springs to fail after repeated use. This could lead to the device not functioning properly during use.
The design change in the load-bearing quick release buckle makes the springs susceptible to fatigue failure after repeated use. This could cause the device to malfunction during operation, but it does not pose an immediate risk of injury.
Users of the Rifton TRAM Standard Base powered lift device with specific ID codes listed in the recall are affected. The risk is low as the failure is related to repeated use and not immediate danger.
Check your Rifton TRAM Standard Base powered lift device for the SKU K310 and specific ID codes listed in the recall. The affected units have unique identification codes starting with K31020120704AA and ending with K31020160825AE.
Verify your device has the SKU K310 and one of the specific ID codes listed in the recall.
The recall number is not provided in the official notice.
Check your device for the SKU K310 and one of the specific ID codes listed in the recall.
No action is needed if your device does not have the specific ID codes listed in the recall.
We’ve drafted a message you can send Community Products to request your refund or repair — edit it as you like.
Subject: Recall Z-0164-2020 — Community Products Community Products Hello, I own a Community Products that is covered by recall Z-0164-2020 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.
