{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Schaumburg",
      "address_1": "1501 E Woodfield Rd",
      "reason_for_recall": "Labeling: Missing label",
      "address_2": "Suite 300 East",
      "product_quantity": "155,900 vials domestically",
      "code_info": "Lot  6004889, Expiration Date 10/2014",
      "center_classification_date": "20130313",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "CALCIUM GLUCONATE INJECTION, USP, 10% (100 mg/mL), 10 mL, Single Dose Vial, Rx only, For Direct Slow IV or IV Additive Use Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- Product Code 31110, NDC 63323-311-10",
      "report_date": "20130320",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Fresenius Kabi USA LLC (FK USA)",
      "recall_number": "D-200-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "64266",
      "termination_date": "20131118",
      "more_code_info": "",
      "recall_initiation_date": "20130201",
      "postal_code": "60173-6052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}