Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Reported: November 29, 2017 Initiated: September 10, 2017 #Z-0111-2018
Product Description
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.
Details
- Recalling Firm
- Medtronic Inc.
- Units Affected
- 5,842 units
- Distribution
- Worldwide
- Location
- Northridge, CA
Frequently Asked Questions
What product was recalled? ▼
Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281). Recalled by Medtronic Inc.. Units affected: 5,842 units.
Why was this product recalled? ▼
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 29, 2017. Severity: Moderate. Recall number: Z-0111-2018.
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