Medtronic Inc. recalls Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)
- Recall date
- September 10, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0108-2018
- 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) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)
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