{
  "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": [
    {
      "status": "Terminated",
      "city": "Levittown",
      "state": "PA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72819",
      "recalling_firm": "Bio-pharm, Inc.",
      "address_1": "2091 Hartel Ave",
      "address_2": "N/A",
      "postal_code": "19057-4506",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-0809-2016",
      "product_description": "Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5 mL), 16 fl oz Bottle, Rx only, Mfd For: Heritage Pharmaceuticals Inc., Eatontown, NJ 07724, NDC 23155-291-51",
      "product_quantity": "103,664 Bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.",
      "recall_initiation_date": "20151217",
      "center_classification_date": "20160401",
      "termination_date": "20170508",
      "report_date": "20160413",
      "code_info": "Lot #s: 14G008, 14G013, 14G010, 14G015, 14G016, 14G021, 14G026,  14G028, Exp. 01/2016; 14K027, 14K023, Exp. 04/2016; 15B040, 15B041, Exp. 08/2016; 15E042, Exp. 11/2016; 15F019, 15F021, Exp. 12/2016; 15G038, Exp. 01/2017; 15H004, 15H008, Exp. 02/2017",
      "more_code_info": ""
    }
  ]
}