Reported Nov 29, 2017 · Ongoing
Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T,…
Medtronic Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Inc. · 18000 Devonshire St · Northridge, CA · 91325-1219
Is this the product you have?
Medtronic MiniMed(TM) Mio(TM) (MMT-921921T923923T925925T941941T943943T945945T961963963T965965T975975T)
- Lot codes and dates
- Lot Numbers
1,437 of 1,437 codes
507967250796745079675507969750796985082268508262250827735084125508446050844645085187508697450875865088981509130550950685095069509517750951955097241509796750982255101297510162451033115103312510340951038885104247510463251061855109341510970251097075109788510978951097905109791511544051154565117215511793551192335119933512217351223985123224512322851232535123254512787051279325129136513006451300845131255513185351318545132018
- Lot Numbers
- Amount recalled
- 1,513,530 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Why it was recalled
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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