Reported Jan 28, 2026 · Ongoing

Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height…

Community Products, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Community Products, LLC · 2032 Route 213 · Rifton, NY · 12471

Is this the product you have?

  • Rifton Equipment, E-Pacer
  • Model/Catalog NumberK660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion
Lot codes and dates
  • Model/Catalog NumberK660
  • ID Codes

    478 of 478 codes

    • K66020170425AA
    • K66020170612AA
    • K66020170621AA
    • K66020170622AA
    • K66020170626AA
    • K66020170626AB
    • K66020170626AC
    • K66020170627AC
    • K66020170627AD
    • K66020170628AA
    • K66020170629AA
    • K66020170703AA
    • K66020170705AA
    • K66020170711AA
    • K66020170712AA
    • K66020170712AC
    • K66020170713AB
    • K66020170716AA
    • K66020170717AA
    • K66020170717AB
    • K66020170804AA
    • K66020170805AA
    • K66020170807AA
    • K66020170810AA
    • K66020170810AB
    • K66020170811AA
    • K66020170811AC
    • K66020170815AA
    • K66020170817AC
    • K66020170818AC
    • K66020170831AA
    • K66020170831AB
    • K66020170906AA
    • K66020170906AB
    • K66020170911AA
    • K66020170911AB
    • K66020170911AC
    • K66020170913AA
    • K66020170914AA
    • K66020170915AA
    • K66020170921AA
    • K66020170923AA
    • K66020170926AA
    • K66020170927AA
    • K66020170928AA
    • K66020171004AA
    • K66020171006AA
    • K66020171006AB
    • K66020171007AA
    • K66020171010AA
    • K66020171010AB
    • K66020171019AA
    • K66020171020AA
    • K66020171024AA
    • K66020171026AA
    • K66020171026AB
    • K66020171026AC
    • K66020171028AA
    • K66020171030AA
    • K66020171101AA
Amount recalled
470 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for fraying on the body support strap.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:42 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.