Official recall record
Paradigm and MiniMed 600 and 700 series pumps
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-02-26
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
As part of the testing for the Alternate Controller Enabled (ACE) device submission, the R&D team tested the Minimed 780g Insulin Pump at elevated and lowered height conditions relative to the infusion site per the engineering test report. The results of the testing showed that there is an unintended over or under delivery of insulin that occurs when the 780g pump is either elevated or lowered relative to the infusion site.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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