{
  "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": "Huntsville",
      "address_1": "150 Vintage Dr NE",
      "reason_for_recall": "Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.",
      "address_2": "",
      "product_quantity": "360 Bottles",
      "code_info": "Lot #: 52217, Expiry: 04/18",
      "center_classification_date": "20150820",
      "distribution_pattern": "U.S. Including: OH",
      "state": "AL",
      "product_description": "AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland Ltd., Clonmel, Ireland, NDC:  67253-180-50",
      "report_date": "20150826",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals",
      "recall_number": "D-1350-2015",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "71980",
      "termination_date": "20150821",
      "more_code_info": "",
      "recall_initiation_date": "20150813",
      "postal_code": "35811-8216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}