FDA Recall Terminated

MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712.

Recall: Z-1890-2017 · Initiated January 31, 2017

Recall

Recall Number
Z-1890-2017
Event Number
76436
Firm
Medtronic Inc.
FEI Number
3003166194
Status
Terminated
Root Cause
Software design
Initiated
January 31, 2017
Posted
April 28, 2017
Terminated
May 4, 2017
Address
18000 Devonshire Street, Northridge, CA, 91325-1219

Description

MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712.

Reason

Medtronic has identified a software anomaly that can prevent the internal battery of the pump from charging. When the software anomaly occurs it leads to battery depletion and pump shutdown.

Action

A urgent medical device recall letter was sent to customers on 1/31/17 to inform them that Medtronic has identified a software issue that could prevent the internal battery of the pump from charging. Customers are informed that should the software issue occur, an alarm is triggered and they will see the following message displayed on the pump screen: "Power error detected 00:00 25 Delivery stopped. Record your settings by uploading to CareLink or write your settings on paper. See user guide. OK." Customers are informed that If they experience the alarm and see the Power error detected message on their pump accompanied by the number 25, then they are instructed to contact the Medtronic HelpLine team at XXXXX for assistance with troubleshooting the error.

Distribution

Europe, Australia, Japan, Singapore

Quantity

42,215 units