{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76772",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "2 Scimed Pl",
      "address_2": "N/A",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, FL, KY, MO, NM, OK, OR, PA, and TX.",
      "recall_number": "Z-2645-2017",
      "product_description": "Boston Scientific Imager II Angiographic Catheter, a pathway for delivering contrast media to selected sites in the vascular system. M001314141 (5-pack outer package UPN), M001314140, single unit, inner package UPN)",
      "product_quantity": "39 boxes of 5 (195 units)",
      "reason_for_recall": "A field report indicated some units within this lot were missing the bottom pouch seal.  The compromised seal is completely missing and is obvious to the user.",
      "recall_initiation_date": "20161215",
      "center_classification_date": "20170630",
      "termination_date": "20180410",
      "report_date": "20170712",
      "code_info": "Lot:  00112758, Use by 2018-05-11"
    }
  ]
}