{
  "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": "Maple Grove",
      "address_1": "1 Scimed Pl",
      "reason_for_recall": "A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm guidewires.",
      "address_2": "",
      "product_quantity": "49 units",
      "code_info": "Material Number (UPN) H749M3004A0, Batch Number 21558994, Expiration Date 11/30/2019",
      "center_classification_date": "20190220",
      "distribution_pattern": "Nationwide distribution to AR, CT, FL, IA, IL, IN, KY, MA, MI, ND, NJ, NY, OH, OK, PA, SC, TX, VA, WI, WY.",
      "state": "MN",
      "product_description": "Stingray\" Guidewire, labeled as 300cm.  intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).",
      "report_date": "20190227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Boston Scientific Corporation",
      "recall_number": "Z-0852-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81863",
      "termination_date": "20200609",
      "more_code_info": "",
      "recall_initiation_date": "20181219",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}