Reported Jul 20, 2022 · Ongoing
MiniMed 720G Insulin Pump (O.U.S. Version)
Medtronic MiniMed
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 MiniMed · 18000 Devonshire St · Northridge, CA · 91325-1219
Is this the product you have?
- MiniMed 720G Insulin Pump (O.U.S. Version)
- Lot codes and dates
- Product Number/CFN (O.U.S. Version) MiniMed 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1817
- MMT-1867) UDI CodesPending Serial Numbers (O.U.S.)
575 of 575 codes
NG2820120HNG2820133HNG2820138HNG2820180HNG2820183HNG2820193HNG2820227HNG2820238HNG2820239HNG2820241HNG2820242HNG2820253HNG2820256HNG2820258HNG2820282HNG2820295HNG2820339HNG2820341HNG2820357HNG2820366HNG2820368HNG2820371HNG2820372HNG2820374HNG2820377HNG2820379HNG2820381HNG2820386HNG2820387HNG2820388HNG2820393HNG2820394HNG2820396HNG2820398HNG2820400HNG2820401HNG2820409HNG2820418HNG2820421HNG2820425HNG2820428HNG2820432HNG2820435HNG2820437HNG2820457HNG2820460HNG2820462HNG2820463HNG2820467HNG2820472HNG2820484HNG2820487HNG2820489HNG2820494HNG2820496HNG2820498HNG2820501HNG2820503HNG2820510HNG2820512H
- Amount recalled
- 575 pumps
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
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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