Drug recall
Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment
FDA recall event 95233 · Class II · Btt Health Gmbh
Key facts
| Event ID | 95233 |
|---|---|
| Recall numbers | Z-3162-2024 |
| Recalling firm | Btt Health Gmbh |
| Product type | Devices |
| Products | Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Aug 1, 2024 |
| Report date | Sep 25, 2024 |
| City | Inning |
| Country | Germany |
| FEI number | 3013515165 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: