{
  "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": "2026-07-29",
    "results": {
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    {
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      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
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        "nui": [
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        "pharm_class_moa": [
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        "pharm_class_epc": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "90594",
      "recalling_firm": "Teva Pharmaceuticals USA Inc",
      "address_1": "400 Interpace Pkwy Bldg A",
      "address_2": "",
      "postal_code": "07054-1120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in Ohio",
      "recall_number": "D-1334-2022",
      "product_description": "Azacitidine for Injection 100mg/vial Lyophilized Powder, Rx Only, Mfd. in Romania By: Sindan Pharma SRL For BluePoint Laboratories, NDC 68001-313-56",
      "product_quantity": "4162 cartons",
      "reason_for_recall": "Subpotent Drug - Out of specification (OOS) result obtained during monitoring stability study for Assay. Results below specification.",
      "recall_initiation_date": "20220722",
      "center_classification_date": "20220811",
      "termination_date": "20230412",
      "report_date": "20220817",
      "code_info": "Lot: FE22001A, Exp 01/2024",
      "more_code_info": ""
    }
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}