{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Dayton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "94528",
      "recalling_firm": "Hikma Injectables USA Inc",
      "address_1": "36 Stults Rd",
      "address_2": "",
      "postal_code": "08810-1540",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0480-2024",
      "product_description": "Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection, packaged in 100mL bags, Rx only, Compounded by: Hikma Injectables USA Inc. 2 Esterbrook Lane, Cherry Hill, NJ 08003, Distributed by: Hikma Injectables USA Inc. 36 Stults Road, Dayton, NJ 08810, NDC 63037-100-05",
      "product_quantity": "1,895 bags",
      "reason_for_recall": "Labeling: Wrong Barcode",
      "recall_initiation_date": "20240430",
      "center_classification_date": "20240502",
      "report_date": "20240508",
      "code_info": "Lot #: CH0324001, Exp. Date 3/4/2025",
      "more_code_info": ""
    }
  ]
}