Reported Oct 30, 2019 · Terminated

Rifton E-Pacer, SKU K660, powered lift device

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 E-Pacer, SKU K660, powered lift device
Lot codes and dates
  • ID Codes

    118 of 118 codes

    • K66020170425AA
    • K66020170612AA
    • K66020170621AA
    • K66020170622AA
    • K66020170626AA
    • K66020170626AB
    • K66020170626AC
    • K66020170627AC
    • K66020170627AD
    • K66020170628AA
    • K66020170629AA
    • K66020170703AA
    • K66020170705AA
    • K66020170711AA
    • K66020170712AA
    • K66020170712AC
    • K66020170713AB
    • K66020170713AC
    • K66020170716AA
    • K66020170717AA
    • K66020170717AB
    • K66020170804AA
    • K66020170805AA
    • K66020170807AA
    • K66020170810AA
    • K66020170810AB
    • K66020170811AA
    • K66020170811AC
    • K66020170815AA
    • K66020170817AB
    • 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
Amount recalled
167

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

A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.

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

Notice updated Jun 15, 2020 · Data as of Sep 19, 5:31 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.