Reported Nov 29, 2017 · Ongoing

Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)

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 St · Northridge, CA · 91325-1219

Is this the product you have?

  • Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)
Lot codes and dates
  • Lot Numbers

    108 of 108 codes

    • 5179979
    • 5182542
    • 5185471
    • 5187173
    • 5188894
    • 5189581
    • 5191349
    • 5192467
    • 5178077
    • 5189588
    • 5181137
    • 5181140
    • 5184757
    • 5184758
    • 5186199
    • 5186203
    • 5188890
    • 5191350
    • 5193510
    • 5186206
    • 5179854
    • 5179857
    • 5179975
    • 5181712
    • 5182176
    • 5182543
    • 5183121
    • 5185154
    • 5185157
    • 5186200
    • 5186201
    • 5186202
    • 5187102
    • 5187170
    • 5188889
    • 5188893
    • 5190033
    • 5190708
    • 5190710
    • 5191351
    • 5192470
    • 5192679
    • 5194101
    • 5168207
    • 5189592
    • 5175824
    • 5176442
    • 5179855
    • 5179977
    • 5181711
    • 5181713
    • 5182177
    • 5182179
    • 5182544
    • 5183122
    • 5183123
    • 5184087
    • 5185155
    • 5185156
    • 5187101
Amount recalled
1,898,570 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Why it was recalled

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

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

Data as of Sep 19, 4:45 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.