MiniMed 770G Insulin Pump (U.S. and O.U.S. Version)
Check against the official notice below — it lists the full affected range.
Medtronic is recalling approximately 123,585 MiniMed 770G insulin pumps distributed across the United States and other markets. The pumps are affected by battery cap deterioration that may cause an incomplete battery circuit, resulting in loss of power and functionality of the insulin infusion pumps. The recall affects specific product numbers (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892) and includes pumps with particular serial numbers beginning with "NG" followed by numbers and the letter "H."
The recall notice does not specify a remedy or instructions for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Reason for recall: 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. Distribution: 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 Quantity: 123,585 pumps Lot/code info: Product Number/CFN (U.S. and O.U.S. Version) MiniMed" 770G pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892) UDI-DI Codes: 763000413750 763000439866 763000414344 763000439859 Serial Numbers: U.S. NG2574462H NG2507207H NG2591910H NG2450722H NG2909394H NG2562452H NG2773622H NG2747513H NG2499718H NG2871000H NG3039842H NG2962106H NG2522230H NG2752787H NG2613810H NG2583058H NG2491224H NG2581838H NG2603110H NG2463710H NG2497307H NG2514402H NG2713369H NG2823275H NG2495711H NG2456706H NG2546535H NG2811181H NG2642457H NG2542689H NG2878631H NG2533834H NG2614812H NG2656169H NG2530373H NG2614196H NG2656857H NG2488084H NG2644432H NG2641394H NG2922162H NG2583381H NG2982740H NG2659486H NG2635500H NG2773665H NG2750822H NG2569688H NG2719815H NG2509897H NG2593191H NG2613613H NG2509074H NG2642600H NG2498351H NG2467403H NG2614448H NG2446285H NG2787601H NG3040387H NG2534927H NG2968936H NG2912599H NG2616916H NG2512410H NG2672631H NG2562612H NG2542395H NG2752089H NG2869829H NG2495443H NG2918939H NG2515111H NG2455735H NG2940622H NG2981974H NG3001236H NG2643877H NG2710575H NG2473962H NG2536175H NG2633328H NG2869784H NG2467347H NG2542341H NG2951926H NG2614312H NG2581561H NG2577607H NG2774627H NG2650858H NG2493876H NG2545251H NG2551254H NG2699398H NG2573878H NG2507390H NG2952926H NG2506869H NG2550514H NG2541661H NG2761100H NG2583123H NG2699493H NG2962387H NG2636697H NG2544910H NG2495683H NG2873468H NG3002826H NG2674336H NG2636561H NG2544472H NG2450627H NG2981283H NG2777421H NG2487458H N
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.