{
  "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
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  },
  "results": [
    {
      "country": "United States",
      "city": "Schaumburg",
      "address_1": "1901 N Roselle Rd Ste 700",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: High out of specification results for an impurity.",
      "address_2": "",
      "product_quantity": "205,370 vials",
      "code_info": "Lot #: AJM601, Exp. Jul-2018; AJM701, AJM702, Exp. Dec-2018",
      "center_classification_date": "20180312",
      "distribution_pattern": "Nationwide in the USA.",
      "state": "IL",
      "product_description": "methylPREDNISolone Sodium Succinate for Injection, USP, 40 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-807-05.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sagent Pharmaceuticals Inc",
      "recall_number": "D-0586-2018",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Drugs",
      "event_id": "79419",
      "termination_date": "20200415",
      "more_code_info": "",
      "recall_initiation_date": "20180305",
      "postal_code": "60195-3194",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}