Community Products recalls E-Pacer K660 gait training devices due to potential body support strap fraying. Check ID codes listed for affected units.
Potential for fraying on the body support strap.
Community Products is recalling E-Pacer K660 gait training devices because the body support strap may fray. This could cause the device to become unstable during use, especially for people who need assistance with standing and sitting.
The body support strap may fray over time, which could cause the device to become unstable during use. This instability might lead to falls or injuries, particularly when the user is moving between sitting and standing positions.
People who own or use the E-Pacer K660 gait training device with power height adjustment are most at risk. This includes individuals using the device for sit-to-stand motions, such as those with mobility challenges.
Check for the model number K660 on the device or the ID codes listed in the recall notice. The affected units have specific ID codes starting with K6602017 and ending with various combinations of letters and numbers.
Inspect the body support strap for any signs of fraying or damage before using the device.
If the strap shows fraying, stop using the device immediately and contact Community Products for further instructions.
The E-Pacer K660 is a gait training device with power height adjustment that helps users move between sitting and standing positions.
Check the model number on the device or look for the ID codes listed in the recall notice, which start with K6602017 and have specific combinations of letters and numbers.
Stop using the device immediately and contact Community Products for further instructions.
We’ve drafted a message you can send Community Products to request your refund or repair — edit it as you like.
Subject: Recall Z-1139-2026 — Community Products Community Products Hello, I own a Community Products that is covered by recall Z-1139-2026 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.
