Reported Nov 29, 2017 · Ongoing

Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)

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) Pro-set(TM) (MMT-280
    • 281)
Lot codes and dates
  • Lot Numbers
    • 6211649
    • 6207537
Amount recalled
5,842 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.

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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, 5:27 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.