# FDA recall Z-3162-2024

> **Btt Health Gmbh** · Class II · device recall initiated 2024-08-01.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-3162-2024
- **Recalling firm:** Btt Health Gmbh
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-01
- **Report date:** 2024-09-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Inning, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3162-2024

## Citation

> AI Analytics. FDA recall Z-3162-2024. Retrieved 2026-09-25 from https://api.ai-analytics.org/recall/Z-3162-2024. Source: US FDA. Licensed CC0.

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