{
  "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": "ACCOLADE SR model L300, ACCOLADE DR model L301, ACCOLADE MRI SR model L310, ACCOLADE  MRI DR model L311, ACCOLADE EL DR model L321 and ACCOLADE MRI EL DR model L331.",
      "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": "ACCOLADE Pacemaker",
      "report_date": "20181003",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Boston Scientific Corporation",
      "recall_number": "Z-3257-2018",
      "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"
    }
  ]
}