{
  "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": "275 N Field Dr",
      "reason_for_recall": "Superpotent; Cartridges labeled to contain 1 mL found to contain 2.2 mL",
      "address_2": "",
      "product_quantity": "212,370 cartidges",
      "code_info": "Lot #10830LL, Exp. 1APR2013",
      "center_classification_date": "20120715",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "Morphine Sulfate Injection, USP,  4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit with Luer Lock, packaged 10 Carpujects/carton, CII, Rx only, Hospira, Inc., Lake Forest, IL  ---- NDC 0409-1258-30",
      "report_date": "20120725",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "D-1419-2012",
      "initial_firm_notification": "Press Release",
      "product_type": "Drugs",
      "event_id": "61624",
      "termination_date": "20150529",
      "more_code_info": "",
      "recall_initiation_date": "20120417",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}