Home › Device types › MHZ
Stimulator, Vestibular Acceleration, Therapeutic
FDA product code MHZ · Class 3 · Unknown
0
Registered devices
3
Adverse events
2
Recalls
1
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-08-31 | GE Healthcare, LLC | The patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time. |
| 2010-04-14 | Spacelabs Healthcare, Incorporated | There have been reports that the Spacelabs Medical Vital Signs Monitor, Model 91220, will not power up with AC power and will no longer charge the batteries. |
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