FDA Device recall Z-1890-2017

MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected

FDA Device
Class II
terminated
Published 2017-05-10

On 2017-05-10 the FDA classified a Class II recall of MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected by Medtronic, citing 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 pum….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1890-2017
Classification	Class II
Status	terminated
Initiated	2017-01-31
Published	2017-05-10
Last updated	2026-09-13 11:54 UTC
Company	Medtronic
Distribution	n/a

Product

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.

Identifiers

code_info	Serial Numbers NG1000069H NG1000070H NG1000074H NG1000077H NG1000079H NG1000080H NG1000082H NG1000085H NG10000… Serial Numbers NG1000069H NG1000070H NG1000074H NG1000077H NG1000079H NG1000080H NG1000082H NG1000085H NG1000086H NG1000088H NG1000089H NG1000090H NG1000091H NG1000093H NG1000094H NG1000097H NG1000099H NG1000101H NG1000105H NG1000107H NG1000109H NG1000110H NG1000114H NG1000116H NG1000117H NG1000125H NG1000127H NG1000132H NG1000133H NG1000138H NG1000140H NG1000142H NG1000147H NG1000155H NG1000159H NG1000160H NG1000162H NG1000165H NG1000167H NG1000170H NG1000171H NG1000175H NG1000176H NG1000182H NG1000183H NG1000184H NG1000192H NG1000195H NG1000198H NG1000200H NG1000201H NG1000202H NG1000203H NG1000204H NG1000209H NG1000212H NG1000213H NG1000214H NG1000223H NG1000225H NG1000229H NG1000230H NG1000232H NG1000236H NG1000237H NG1000238H NG1000239H NG1000242H NG1000245H NG1000250H NG1000252H NG1000255H NG1000258H NG1000260H NG1000264H NG1000267H NG1000268H NG1000269H NG1000270H NG1000271H NG1000273H NG1000274H

code_info

Serial Numbers NG1000069H NG1000070H NG1000074H NG1000077H NG1000079H NG1000080H NG1000082H NG1000085H NG10000…

Serial Numbers NG1000069H NG1000070H NG1000074H NG1000077H NG1000079H NG1000080H NG1000082H NG1000085H NG1000086H NG1000088H NG1000089H NG1000090H NG1000091H NG1000093H NG1000094H NG1000097H NG1000099H NG1000101H NG1000105H NG1000107H NG1000109H NG1000110H NG1000114H NG1000116H NG1000117H NG1000125H NG1000127H NG1000132H NG1000133H NG1000138H NG1000140H NG1000142H NG1000147H NG1000155H NG1000159H NG1000160H NG1000162H NG1000165H NG1000167H NG1000170H NG1000171H NG1000175H NG1000176H NG1000182H NG1000183H NG1000184H NG1000192H NG1000195H NG1000198H NG1000200H NG1000201H NG1000202H NG1000203H NG1000204H NG1000209H NG1000212H NG1000213H NG1000214H NG1000223H NG1000225H NG1000229H NG1000230H NG1000232H NG1000236H NG1000237H NG1000238H NG1000239H NG1000242H NG1000245H NG1000250H NG1000252H NG1000255H NG1000258H NG1000260H NG1000264H NG1000267H NG1000268H NG1000269H NG1000270H NG1000271H NG1000273H NG1000274H

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1890-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.