MiniMed 670G 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 279,251 MiniMed 670G insulin pumps distributed throughout the United States due to battery cap deterioration. The deteriorating battery cap may cause an incomplete battery circuit, resulting in loss of power and functionality of the insulin infusion pump. The recall affects both U.S. and overseas versions of the device, with specific product numbers, UDI codes, and serial numbers identified in the recall notice.
The recall record does not specify what affected consumers should do regarding this recall.
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: 279,251 pumps Lot/code info: Product Number/CFN (O.U.S. Version) MiniMed 670G (MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1883, MMT-1893) UDI-DI Codes: 643169946040 763000278427 763000179649 643169946057 763000096984 763000190453 763000283445 763000395858 763000367084 643169939202 763000166526 763000256821 763000283506 763000283513 763000365882 643169939219 763000090203 763000190460 763000283520 763000393786 Serial Numbers: U.S. NG1839499H NG1383785H NG2337855H NG2574462H NG2148562H NG1139337H NG2507207H NG1737004H NG1259251H NG2164126H NG2591910H NG1774415H NG2450722H NG2341546H NG2394493H NG1268923H NG2059875H NG1241089H NG2909394H NG2716073H NG1188783H NG1332358H NG1805098H NG1187471H NG1928485H NG2154209H NG2562452H NG1980564H NG1844854H NG1993223H NG2208062H NG1256182H NG2108291H NG2773622H NG2840625H NG2287463H NG2116702H NG2747513H NG2006685H NG2499718H NG2256617H NG1708020H NG2473735H NG2871000H NG2031708H NG3039842H NG2843313H NG2059984H NG2440836H NG1775459H NG2154899H NG2962106H NG2844148H NG1504738H NG1777013H NG2522230H NG2783673H NG1810845H NG2787724H NG2397399H NG2752787H NG2126568H NG2003985H NG1847235H NG1639171H NG2284063H NG2613810H NG2004335H NG2112005H NG2372862H NG1596755H NG2496614H NG2640743H NG2242002H NG2344097H NG1820434H NG2035194H NG2083253H NG2583058H NG2458619H NG2383667H NG2354215H NG2253618H NG2781208H NG2244550H NG2105867H NG1965419H NG2712797H NG2491224H NG2185247H NG2581838H NG2363328H NG2603110H NG2809205H NG2463710H
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.