Medtronic Recalls MiniMed Insulin Pumps for Incorrect Insulin Dosing

Date: 10/05/2021

Product type: Medical Device

Recalled Product

• MiniMed™ 600 Series Insulin Pumps
• Lot codes: Refer to the Medical Device Recalls database entry for each product.
• Distribution Dates:
  • Model 630G – September 2016 to February 2020
  • Model 670G – May 2015 to December 2020
• Devices Recalled in the U.S.: 463,464
• Date Initiated by Firm: November 21, 2019

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-minimed-insulin-pumps-incorrect-insulin-dosing