Home › Insulet Corporation › Omnipod Discover
Omnipod Discover
Insulet Corporation · Model B010-D-DP · UDI-DI 10385083000152
1
510(k) clearances
2,081
Adverse events
2
Recalls
16
Facilities
Description
Omnipod Data Management System
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-21 | Medtronic MiniMed, Inc. | Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect data displayed |
| 2016-08-05 | Medtronic Inc. | Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error. |
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 docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.