Reported Oct 30, 2019 · Terminated

Rifton TRAM Standard Base, SKU K310, 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 Standard Base, SKU K310, powered lift device
Lot codes and dates
  • ID Codes

    2,037 of 2,037 codes

    • K31020120704AA
    • K31020120706AA
    • K31020120707AC
    • K31020120707AD
    • K31020120707AE
    • K31020120707AG
    • K31020120709AA
    • K31020120709AB
    • K31020120709AD
    • K31020120709AE
    • K31020120710AA
    • K31020120710AB
    • K31020120710AE
    • K31020120711AA
    • K31020120711AB
    • K31020120712AA
    • K31020120712AB
    • K31020120713AB
    • K31020120713AC
    • K31020120713AD
    • K31020120713AE
    • K31020120713AF
    • K31020120718AA
    • K31020120718AB
    • K31020120718AC
    • K31020120719AC
    • K31020120720AA
    • K31020120727AA
    • K31020120727AB
    • K31020120801AA
    • K31020120804AB
    • K31020120804AC
    • K31020120804AD
    • K31020120804AH
    • K31020120804AI
    • K31020120806AA
    • K31020120806AB
    • K31020120806AC
    • K31020120806AD
    • K31020120806AE
    • K31020120806AG
    • K31020120806AH
    • K31020120806AI
    • K31020120806AK
    • K31020120806AL
    • K31020120806AM
    • K31020120806AN
    • K31020120806AO
    • K31020120807AA
    • K31020120807AB
    • K31020120807AC
    • K31020120807AD
    • K31020120807AE
    • K31020120807AF
    • K31020120809AD
    • K31020120809AE
    • K31020120810AC
    • K31020120813AB
    • K31020120813AE
    • K31020120814AA
Amount recalled
3282

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.

Free recall alerts

Get alerted about new Community Products, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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, 4:47 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.