{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72855",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "4100 Hamline Ave N",
      "address_2": "N/A",
      "postal_code": "55112-5700",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International Distribution to countries of: COLOMBIA, JAMAICA, TRINIDAD & TOBAGO.",
      "recall_number": "Z-0620-2016",
      "product_description": "Boston Scientific, MRI PROPONENT\" SR , REF L210 Pacemaker.    These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary",
      "product_quantity": "5",
      "reason_for_recall": "The literature packet packaged with the devices incorrectly describes the pacemaker as SR when it is actually a DR pacemaker or DR when it is actually a SR pacemaker.",
      "recall_initiation_date": "20151210",
      "center_classification_date": "20160108",
      "termination_date": "20160308",
      "report_date": "20160120",
      "code_info": "Serial numbers 702961, 702963, 705644, 705666, and 705947."
    }
  ]
}