{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Northridge",
      "address_1": "18000 Devonshire St",
      "reason_for_recall": "Medtronic is recalling the Medtronic Paradigm Insulin Pump because the pump's drive support cap may become detached from the pump case and protrude from the lower right side of the pump.  When the pump is expose to water it may result in damage to the pump's internal electronics.  This moisture damage can prevent the pump's buttons from working properly or can cause the pump to alarm.",
      "address_2": "",
      "product_quantity": "428,000 units",
      "code_info": "Not available",
      "center_classification_date": "20130410",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) the countries of:  AE, AR, AT, AU, BA, BH, BM, BR, BS, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK,  DO, DZ, EC, EE, EG, ES, FI, FR, GB, GR, GT, HK, HR, HU, IE, IL, IN, IQ, IT, JO, JP, KR, KW, LB, LC, LV, MK, MX, MY, NL, NO, NZ, OM, PA, PE, PL, PR, PY, QA, RO, SA, SE, SG, SI, SK, SV, SY, TF, TH, TR, TT, TW, UA, UY, VE, ZA.",
      "state": "CA",
      "product_description": "Medtronic MiniMed Paradigm Insulin Infusion Pumps    Model Numbers: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K, MMT-723, MMT-723K, MMT-554, and MMT-754.    Product Usage:  Paradigm insulin infusion pumps are intended for use to deliver basal and bolus insulin to persons with diabetes.",
      "report_date": "20130417",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic MiniMed",
      "recall_number": "Z-1085-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64754",
      "termination_date": "20131104",
      "more_code_info": "",
      "recall_initiation_date": "20130322",
      "postal_code": "91325-1219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}