{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "600 N Field Dr Bldg J45",
      "reason_for_recall": "CGMP Deviations: Shipment of product not approved for release.",
      "address_2": "",
      "product_quantity": "1,296 units",
      "code_info": "Lot 16-836-FW, Exp 04/14",
      "center_classification_date": "20130322",
      "distribution_pattern": "NC",
      "state": "IL",
      "product_description": "Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09",
      "report_date": "20130403",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Hospira, Inc.",
      "recall_number": "D-215-2013",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "63242",
      "termination_date": "20130328",
      "more_code_info": "",
      "recall_initiation_date": "20120621",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}