{
  "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": "Lake Forest",
      "address_1": "600 N Field Dr",
      "reason_for_recall": "Crystallization",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Lot 38-135-DK, 38-136-DK Exp. Date 1FEB2016;  Lots 44-075-DK, 44-356-DK Exp. Date 1AUG2016;   Lots 44-357-DK, 44-358-DK Exp. Date 1AUG2016;  Lot 46-308-DK Exp. Date 1OCT2016  - Note: The lot number may be followed by additional numbers from 01 to 99    NOVAPLUS label  Lot 38-137-DK Exp. Date 1FEB2016  - Note: The lot number may be followed by additional numbers from 01 to 99",
      "center_classification_date": "20150428",
      "distribution_pattern": "Nationwide, Puerto Rico and Guam.",
      "state": "IL",
      "product_description": "Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3796-01 --- Also labeled under NOVAPLUS label NDC 00409-3796-49",
      "report_date": "20150506",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "D-0973-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "71002",
      "termination_date": "20171204",
      "more_code_info": "",
      "recall_initiation_date": "20150413",
      "postal_code": "60045-4835",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}