Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment
Reported: September 25, 2024 Initiated: August 1, 2024 #Z-3162-2024
Product Description
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).
Details
- Recalling Firm
- Btt Health Gmbh
- Units Affected
- 62 units
- Distribution
- US Nationwide distribution in the states of Florida.
- Location
- Inning
Frequently Asked Questions
What product was recalled? ▼
Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment. Recalled by Btt Health Gmbh. Units affected: 62 units.
Why was this product 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).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 25, 2024. Severity: Moderate. Recall number: Z-3162-2024.
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