Reported Dec 3, 2025 · Ongoing
CareLink Clinic, REF: MMT-7350
Medtronic MiniMed, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic MiniMed, Inc. · 18000 Devonshire St · Northridge, CA · 91325-1219
Is this the product you have?
- CareLink Clinic
- REFMMT-7350
- Lot codes and dates
- UDI-DI0763000B00008748K
- Software Versions4.2B
- Software Available
US: Between September 4th2025and October 3rd2025
- OUS
Between September 11th2025and October 4th2025
- US (Clinical)
Between August 21st2025and October 3rd2025
- OUS (Clinical)
Between August 21st2025and October 4th2025
- Amount recalled
- 12126
Where it was sold
Why it was recalled
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 on the 24-hour sensor glucose overview graph may lead to hypoglycemia or hyperglycemia.
This product could cause temporary or reversible health problems — stop using it.
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