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Medtronic MiniMed Recall 90370

Description: MiniMed 740G Insulin Pump (O.U.S. Version)

Medtronic MiniMed Recall 90370 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-1357-2022
Event ID90370
Event DescriptionMiniMed 740G Insulin Pump (O.U.S. Version)
Product TypeDevices
DistributionU.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
Quantity40 pumps
Recall ReasonDue 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.
Device Classification20220720
Device Code InfoProduct Number/CFN (O.U.S. Version) MiniMed" 740G pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862) UDI Codes: Pending Serial Numbers (O.U.S.): NG2644996H NG2645006H NG2645007H NG2645013H NG2645014H NG2645023H NG2645025H NG2645026H NG2645030H NG2645032H NG2645051H NG2645062H NG2645065H NG2645066H NG2645067H NG2645074H NG2645077H NG2645081H NG2645086H NG2645097H NG2645100H NG2645101H NG2645115H NG2645116H NG2645117H NG2645119H NG2645120H NG2645122H NG2645125H NG2645127H NG2645128H NG2645139H NG2645143H NG2645146H NG2645148H NG2645150H NG2645151H NG2645164H NG2645178H NG2645213H
Center Classification Date20220708
Recall Initiation Date20220523
Recalling FirmMedtronic MiniMed
Initial Notification Letter
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