{
  "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": "Schaumburg",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "74373",
      "recalling_firm": "Sagent Pharmaceuticals Inc",
      "address_1": "1901 N Roselle Rd Ste 700",
      "address_2": "N/A",
      "postal_code": "60195-3194",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1450-2016",
      "product_description": "Oxacillin for Injection, USP, 10 grams per pharmacy bulk package, Buffered - For IV Use, Sterile, Nonpyrogenic, Preservative-free, Rx Only, Mfd for Sagent Pharmaceuticals, Schaumberg, IL, 60196, USA, Made in India, NDC 25021-163-69",
      "product_quantity": "3990 vials",
      "reason_for_recall": "Presence of Particulate Matter; The firm received two product complaints for small, dark particulate matter identified in solution post reconstitution.",
      "recall_initiation_date": "20160613",
      "center_classification_date": "20160728",
      "termination_date": "20170922",
      "report_date": "20160803",
      "code_info": "Lot #: OXT515, Exp. July 2017"
    }
  ]
}