Home › Device types › MPR
Stent, Bladder, Fetal
FDA product code MPR · Class f · Unknown
1
Registered devices
26
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-08-01 | Rocket Medical Plc | A complaint was received regarding kinking of the device prior to use. If a device is kinked it cannot be used. In addition, the company became aware that the d |
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