Medtronic MiniMed Medtronic MiniMed Paradigm Model 712 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic MiniMed Paradigm Model 712
Brand
Medtronic MiniMed
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Paradigm model 712pumps with serial numbers that end in '-Dxx3' . Where 'x' can be any number or letter.
Medtronic MiniMed is recalling Medtronic MiniMed Paradigm Model 712 due to Several complaints of pumps exhibiting A47 alarms were received. Investigation revealed the alarms occurred when the pump attempted to display text t. 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
Several complaints of pumps exhibiting A47 alarms were received. Investigation revealed the alarms occurred when the pump attempted to display text that exceeded the maximum display length of the pump screen. The investigation revealed this only occurs when the pump is programmed to display information in Spanish.
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