{
  "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": "Saint Paul",
      "address_1": "4100 Hamline Ave N Bldg 3",
      "reason_for_recall": "Boston Scientific has identified a subset of   active pacemaker and CRT-Ps systems with an  elevated potential for early pacemaker replacement due to hydrogen-induced accelerated battery depletion.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "ESSENTIO SR model L100,  ESSENTIO DR model L101, ESSENTIO MRI SR model L110, ESSENTIO MRI DR model L111, ESSENTIO EL DR model L121, and ESSENTIO MRI EL DR model L131",
      "center_classification_date": "20180927",
      "distribution_pattern": "AK, AL, AR, AZ, CA, CO,  CT, 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, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, W A, WI, WV, and WY",
      "state": "MN",
      "product_description": "ESSENTIO Pacemaker",
      "report_date": "20181003",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Boston Scientific Corporation",
      "recall_number": "Z-3255-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81001",
      "termination_date": "20191104",
      "more_code_info": "",
      "recall_initiation_date": "20180910",
      "postal_code": "55112-5700",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}