{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Northridge",
      "address_1": "18000 Devonshire St",
      "reason_for_recall": "There have been reported incidents of a loose reservoir that can no longer be locked into the pump. The reservoir can become loose due to a broken or missing retainer ring that prevents a proper lock. If the reservoir is not properly locked into the pump, it could lead to over or under delivery of insulin, which could then result in hypoglycemia or hyperglycemia.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "All Serial Numbers ( excluding devices with black retainer rings)",
      "center_classification_date": "20200207",
      "distribution_pattern": "US:AK,AL,AR,AZ,BM,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, VT, WA, WI, WV, WY  OUS: France, Germany, UK, Italy, Netherlands, Spain, Sweden, Israel, Norway, Austria, Belgium, Denmark, Czech Republic, Finland, Switzerland, Slovakia, Ireland, Poland, S. Africa, Greece, Hungary, Saudi Arabia, United Arab Emira,  New Zealand, Australia, Japan, Mexico, Colombia, Brazil, S. East Asia, Korea, Canada,",
      "state": "CA",
      "product_description": "Medtronic MiniMed 670G System with SmartGuard, Ref #s/Model Number(s) -  MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781,  and MMT-1782",
      "report_date": "20200219",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Medtronic Inc.",
      "recall_number": "Z-0956-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84430",
      "more_code_info": "",
      "recall_initiation_date": "20191121",
      "postal_code": "91325-1219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}