{
  "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": [
    {
      "status": "Terminated",
      "city": "Amityville",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "70097",
      "recalling_firm": "Hi-Tech Pharmacal Co., Inc.",
      "address_1": "369 Bayview Ave",
      "address_2": "N/A",
      "postal_code": "11701-2801",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NJ, OH, TX, LA, and Puerto Rico",
      "recall_number": "F-1380-2015",
      "product_description": "FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059,  NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701",
      "product_quantity": "581 units",
      "reason_for_recall": "Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.",
      "recall_initiation_date": "20141223",
      "center_classification_date": "20150303",
      "termination_date": "20170508",
      "report_date": "20150311",
      "code_info": "Lot 62110, exp. date 04/2015"
    }
  ]
}