FDA Device Intelligence
HomeDevice 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

DateFirmReason
2019-08-01Rocket Medical PlcA 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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.