International safety notice
Bombas de insulina MiniMed Paradigm 512/712, Bombas de insulina MiniMed Paradigm 515/715, Bombas de insulina MiniMed Paradigm 522/722, Bombas de insulina MiniMed Paradigm Veo 554/754, Bombas de insulina MiniMed 508
Spain / AEMPS · ESP · Jul 26, 2019
Key facts
| Title | Bombas de insulina MiniMed Paradigm 512/712, Bombas de insulina MiniMed Paradigm 515/715, Bombas de insulina MiniMed Paradigm 522/722, Bombas de insulina MiniMed Paradigm Veo 554/754, Bombas de insulina MiniMed 508 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Bombas de insulina MiniMed Paradigm 512/712, Bombas de insulina MiniMed Paradigm 515/715, Bombas de insulina MiniMed Paradigm 522/722, Bombas de insulina MiniMed Paradigm Veo 554/754, Bombas de insulina MiniMed 508 |
| Manufacturer | Medtronic MiniMed, EEUU. |
| Models | 91.822.52.89, 28050, 53284, 28022, 640GBOMBA, 2019-414, FA875 |
| Event type | Safety Notice |
| Date | Jul 26, 2019 |
At a glance
- No Recall
- Yes Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1