Medtronic MiniMed Medtronic MiniMed Model 7311 Version 5.0B Solutions Pumps and Meters Software. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic MiniMed Model 7311 Version 5.0B Solutions Pumps and Meters Software.
Brand
Medtronic MiniMed
Lot Codes / Batch Numbers
All software versions 5.0A and 5.0B
Products Sold
All software versions 5.0A and 5.0B
Medtronic MiniMed is recalling Medtronic MiniMed Model 7311 Version 5.0B Solutions Pumps and Meters Software. due to A minor software anomaly results in an error in the calculation of the average glucose range that appears on one of the reports available in the model. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A minor software anomaly results in an error in the calculation of the average glucose range that appears on one of the reports available in the model 7311 software.
Recommended Action
Per FDA guidance
Firm will send a Product Performance Update in all new shipments of the model 7311 version 5.0B software and it will be provided to all customers already receiving the version B software. When available, version 5.0c will be provided to customers with A or B software.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026