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CareLink™ Personal

MEDTRONIC MINIMED, INC. · Model MMT-7333WW · UDI-DI 00763000424121

PHV
1
510(k) clearances
2,060
Adverse events
2
Recalls
15
Facilities

Description

PRODUCT SFTWR MMT-7333WW PERSONAL 14.13A

Recalls

DateFirmReason
2025-10-21Medtronic 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
2016-08-05Medtronic Inc.Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error.

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

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Data 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.