Reported Oct 30, 2019 · Terminated

Rifton TRAM Low Base, SKU K320, 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 TRAM Low Base, SKU K320, powered lift device
Lot codes and dates
  • ID Codes

    813 of 813 codes

    • K32020130515AA
    • K32020130603AA
    • K32020130606AA
    • K32020130607AA
    • K32020130607AB
    • K32020130610AA
    • K32020130612AA
    • K32020130617AA
    • K32020130617AB
    • K32020130618AA
    • K32020130709AA
    • K32020130713AA
    • K32020130713AB
    • K32020130717AB
    • K32020130730AA
    • K32020130801AA
    • K32020130802AA
    • K32020130802AB
    • K32020130805AA
    • K32020130807AA
    • K32020130808AA
    • K32020130808AB
    • K32020130812AA
    • K32020130812AB
    • K32020130812AC
    • K32020130812AD
    • K32020130813AA
    • K32020130814AA
    • K32020130820AA
    • K32020130822AA
    • K32020130823AA
    • K32020130824AA
    • K32020130827AA
    • K32020130827AB
    • K32020130828AA
    • K32020130830AA
    • K32020130830AB
    • K32020130907AA
    • K32020130909AA
    • K32020130909AB
    • K32020130909AC
    • K32020130909AD
    • K32020130909AE
    • K32020130911AA
    • K32020130912AA
    • K32020130919AA
    • K32020130920AA
    • K32020130920AB
    • K32020130924AA
    • K32020131005AA
    • K32020131007AA
    • K32020131007AB
    • K32020131008AA
    • K32020131009AA
    • K32020131017AB
    • K32020131021AA
    • K32020131022AB
    • K32020131022AC
    • K32020131022AD
    • K32020131024AA
Amount recalled
1079

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.

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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, 6:07 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.