Marodyne-LiV — Class II medical device recall Z-3162-2024
Ongoing recall by Btt Health Gmbh, reported 2024-09-25, distributed nationwide. Some power supply units in Austria and Germany had a voltage drop in the millisecond range, which led to a can
| Recall number | Z-3162-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Btt Health Gmbh, Inning, Germany |
| Recall initiated | 2024-08-01 |
| Classified | 2024-09-17 |
| Reported by FDA | 2024-09-25 |
| Distributed | Nationwide (US) |
| Quantity | 62 units |
| UPC / GTIN / UDI-DI | 05322111240430, 05328511240506, 05336911240521, 05337611240521, 05338311240521, 05339011240521 |
| Model numbers | 3045-133 |
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3162-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.