Reported May 10, 2017 · Terminated

MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these…

Medtronic Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medtronic Inc. · 18000 Devonshire Street · Northridge, CA · 91325-1219

Is this the product you have?

  • 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.
Lot codes and dates
  • Serial Numbers

    2,716 of 2,716 codes

    • 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
Amount recalled
42,215 units

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 4, 2017 · Data as of Sep 19, 4:46 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.