Rifton TRAM Low Base powered lift device (SKU K320) with specific ID codes recalled due to design change making load-bearing buckle susceptible to fatigue failure after repeated use.
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Rifton TRAM Low Base powered lift devices with SKU K320 are being recalled because a design change makes the load-bearing quick release buckle prone to fatigue failure after repeated use. This could lead to the device failing during use, potentially causing injury.
The design change to the load-bearing quick release buckle makes the springs in the latch mechanism susceptible to fatigue failure after repeated use. This means the buckle could become weak and fail unexpectedly, potentially causing the device to malfunction during use.
Users of the Rifton TRAM Low Base powered lift device with SKU K320 are affected. Those who use the device for lifting or moving people are at higher risk of injury if the device fails during use.
Check for the SKU K320 on the device. The specific ID codes listed in the recall include many combinations starting with K32020130515AA through K32020180405AA.
Look for the SKU K320 on the device and check if it matches the specific ID codes listed in the recall.
If you have the recalled device, stop using it immediately to prevent potential failure during use.
Rifton TRAM Low Base powered lift devices with SKU K320 are being recalled due to a design change that makes the load-bearing quick release buckle susceptible to fatigue failure after repeated use.
Check for the SKU K320 on the device and look for the specific ID codes listed in the recall, which include many combinations starting with K32020130515AA through K32020180405AA.
Stop using the device immediately and contact Rifton for further instructions.
We’ve drafted a message you can send Rifton to request your refund or repair — edit it as you like.
Subject: Recall Z-0165-2020 — Rifton Rifton Hello, I own a Rifton that is covered by recall Z-0165-2020 from Rifton. 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.
