Class II

Medical Device Recall: Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment

Btt Health Gmbh · August 1, 2024

Reason for Recall

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).

Distribution

US Nationwide distribution in the states of Florida.

States Affected

NATIONWIDE

Quantity Affected

62 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3162-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.