{
  "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": "Prince George",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63550",
      "recalling_firm": "American Enterprises LLC dba Sterling Gelatin",
      "address_1": "4595 Sandesara Dr",
      "address_2": "N/A",
      "postal_code": "23875-3045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NJ",
      "recall_number": "D-062-2013",
      "product_description": "Limed Bone Gelatin, packaged in six 125 kg fiber drums and labeled in part PO NO.: P8095 GELATIN 75 BLOOM ITEM NO. RM 164.  MADE IN INDIA",
      "product_quantity": "750 kgs",
      "reason_for_recall": "Microbial Contamination of Non-Sterile Products: Product is being recalled due to possible microbial contamination by C. difficile discovered in the raw material.",
      "recall_initiation_date": "20120921",
      "center_classification_date": "20121121",
      "termination_date": "20121128",
      "report_date": "20121128",
      "code_info": "Batch No. SG4704, Exp 02/22/2017."
    }
  ]
}