{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Schaumburg",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "57878",
      "recalling_firm": "App Pharmaceuticals Llc",
      "address_1": "1501 E Woodfield Rd",
      "address_2": "Suite 300 East",
      "postal_code": "60173-6052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution and Puerto Rico",
      "recall_number": "Z-1824-2012",
      "product_description": "HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial,  plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only    To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.",
      "product_quantity": "133,150 vials",
      "reason_for_recall": "CGMP Deviations: Incomplete documentation associated with test results.",
      "recall_initiation_date": "20100520",
      "center_classification_date": "20120619",
      "termination_date": "20120620",
      "report_date": "20120627",
      "code_info": "Lot 406952 (Expiration Date  02/11)"
    }
  ]
}