Reported Sep 25, 2024 · Ongoing

Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment

Btt Health GmbH

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: Btt Health Gmbh · Billerberg 7 · Inning · N/A

Is this the product you have?

  • Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment
Lot codes and dates
  • serial numbers

    62 of 62 codes

    • 010426065891001421S05327911240506
    • 010426065891001421S05328011240506
    • 010426065891001421S05328111240506
    • 010426065891001421S05328211240506
    • 010426065891001421S05328311240506
    • 010426065891001421S05328411240506
    • 010426065891001421S05328511240506
    • 010426065891001421S05328611240506
    • 010426065891001421S05328711240506
    • 010426065891001421S05328811240506
    • 010426065891001421S05328911240506
    • 010426065891001421S05329011240506
    • 010426065891001421S05321911240430
    • 010426065891001421S05322011240430
    • 010426065891001421S05322111240430
    • 010426065891001421S05322211240430
    • 010426065891001421S05322311240430
    • 010426065891001421S05322411240430
    • 010426065891001421S05322511240430
    • 010426065891001421S05322611240430
    • 010426065891000721S05336411240521
    • 010426065891000721S05336511240521
    • 010426065891000721S05336611240521
    • 010426065891000721S05336711240521
    • 010426065891000721S05336811240521
    • 010426065891000721S05336911240521
    • 010426065891000721S05337011240521
    • 010426065891000721S05337111240521
    • 010426065891000721S05337211240521
    • 010426065891000721S05337311240521
    • 010426065891000721S05337411240521
    • 010426065891000721S05337511240521
    • 010426065891000721S05337611240521
    • 010426065891000721S05337711240521
    • 010426065891000721S05337811240521
    • 010426065891000721S05337911240521
    • 010426065891000721S05338011240521
    • 010426065891000721S05338111240521
    • 010426065891000721S05338211240521
    • 010426065891000721S05338311240521
    • 010426065891000721S05338411240521
    • 010426065891000721S05338511240521
    • 010426065891000721S05338611240521
    • 010426065891000721S05338711240521
    • 010426065891000721S05338811240521
    • 010426065891000721S05338911240521
    • 010426065891000721S05339011240521
    • 010426065891000721S05339111240521
    • 010426065891000721S05339211240521
    • 010426065891000721S05339311240521
    • 010426065891000721S05339411240521
    • 010426065891000721S05339511240521
    • 010426065891000721S05339611240521
    • 010426065891000721S05339711240521
    • 010426065891000721S05339811240521
    • 010426065891000721S05339911240521
    • 010426065891000721S05340011240521
    • 010426065891000721S05340111240521
    • 010426065891000721S05340211240521
    • 010426065891000721S05340311240521
Amount recalled
62 units

Where it was sold

  • Nationwide
  • FL

Why it was recalled

Some power supply units in Austria and Germany had a voltage drop in the millisecond range, which led to a cancellation of the treatment and subsequent restart of the medical device. The treatment is only restarted by a step-off/step-on (step-on for activation).

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, 6:30 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.