Reported May 20, 2020 · Ongoing

EVA Floor Lifts, Model Numbers: 400, 450, 600

Handicare AB

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: Handicare AB · Maskinvagen 17 · Lulea, N/A · N/A

Is this the product you have?

  • EVA Floor Lifts
  • Model Numbers
    • 400
    • 450
    • 600
Lot codes and dates
  • All affected models
Amount recalled
997 units

Why it was recalled

After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.

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

Data as of Sep 19, 6:55 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.