FDAFDA · Food and drugs·Recall number Z-0111-2018
Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Published November 29, 2017 · Recall initiated: September 10, 2017
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Medtronic Inc.
- Distributor
- Worldwide
- Lot
- Lot Numbers: 6211649, 6207537
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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