{
  "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": [
    {
      "country": "United States",
      "city": "Indiana",
      "address_1": "625 Kolter Dr",
      "reason_for_recall": "Crystallization",
      "address_2": "Suite 4",
      "product_quantity": "25 vials",
      "code_info": "NDC 61786-0055-01, Lot # B00484449-100914,   Lot # B0062349-121914, Lot # B006655-011415; Expiration Date: 04/01/2016",
      "center_classification_date": "20150409",
      "distribution_pattern": "PA, OK.",
      "state": "PA",
      "product_description": "KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials  repackaged individually inside an amber glass bottle, packaged by RemedyRepack, Indiana, PA, mfg by Hospira, Inc. Lake Forest, IL NDC 61786-0055-01",
      "report_date": "20150415",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "RemedyRepack Inc.",
      "recall_number": "D-0484-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "70549",
      "termination_date": "20150818",
      "recall_initiation_date": "20150218",
      "postal_code": "15701-3570",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}