{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Saint Paul",
      "address_1": "2400 Pilot Knob Rd",
      "reason_for_recall": "Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct strength is displayed on the primary container.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Lot #: 17C01-U07-036096, Exp. 5/1/2020",
      "center_classification_date": "20170503",
      "distribution_pattern": "Nationwide within US",
      "state": "MN",
      "product_description": "Zinc Oxide Paste 25%, 500 g, For Prescription Compounding, Fagron Inc.2400 Pilot Knob Rd, St. Paul, MN 55120m  NDC 51522-0694-5.",
      "report_date": "20170510",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Fagron, Inc",
      "recall_number": "D-0695-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "77018",
      "termination_date": "20170811",
      "more_code_info": "",
      "recall_initiation_date": "20170417",
      "postal_code": "55120-1118",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}