FDA recall Z-0111-2018
Medtronic Inc. · Class II · device
Product
Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Reason for recall
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Distribution
Worldwide
Key facts
- Status
- Ongoing
- Initiation date
- 2017-09-10
- Report date
- 2017-11-29
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Northridge, CA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0111-2018