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CareLink™ MMT-7350Recalls & reported problems

Medtronic Minimed, Inc. · PRODUCT SOFTWARE MMT-7350 PROWEB 3.13A · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Nov 12, 2020Open, Classified

    Incomplete basal rate information may be transmitted leading to a potential for inappropriate change in therapy. During data upload, radio frequency (RF) interference can occur at any point from surrounding devices or equipment that may affect the data transfer between the insulin pump and the CareLink Personal or CareLink System Software.

    Z-0843-2021 · Root cause: Device Design · Recall details · FDA record ↗

Other Continuous glucose monitor retrospective data analysis software devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page