FDA-Device2022-07-20Class II

MiniMed 720G Insulin Pump (O.U.S. Version)

Medtronic MiniMed
Hazard

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.

Sold states
U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV, and WY O.U.S.: Not provided
Affected count
575 pumps
Manufactured in
18000 Devonshire St, Northridge, CA, United States
Products
MiniMed 720G Insulin Pump (O.U.S. Version)

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1356-2022

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief