Medtronic Inc. recalls Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
- Recall date
- September 10, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0107-2018
- FDA classification
- Class II
- Brand / firm
- Medtronic Inc.
- Sold / distributed
- Worldwide
Why it was recalled
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
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