Medtronic MiniMed Ambulatory infusion pump. Model 511 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ambulatory infusion pump. Model 511
Brand
Medtronic MiniMed
Lot Codes / Batch Numbers
No information at this time.
Products Sold
No information at this time.
Medtronic MiniMed is recalling Ambulatory infusion pump. Model 511 due to Non delivery of insulin by pump after electrostatic discharge.. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: corrective action details.
Reason for Recall
As stated by FDA
Non delivery of insulin by pump after electrostatic discharge.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
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