{
  "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 I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "94522",
      "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": "CO, GA, PA, SD, WA",
      "recall_number": "D-0508-2024",
      "product_description": "Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables USA Inc, 36 Stults Road, Dayton, NJ 08810, NDC 63037-123-25",
      "product_quantity": "",
      "reason_for_recall": "Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.",
      "recall_initiation_date": "20240429",
      "center_classification_date": "20240523",
      "report_date": "20240529",
      "code_info": "Lot #: 240310003D, Exp 6/4/2024",
      "more_code_info": ""
    }
  ]
}