{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
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      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        ],
        "generic_name": [
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        "manufacturer_name": [
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        ],
        "product_ndc": [
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          "0409-9093"
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          "0409-9094-12",
          "0409-9094-22",
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        "is_original_packager": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "86074",
      "recalling_firm": "Pfizer Inc.",
      "address_1": "235 E 42nd St",
      "address_2": "",
      "postal_code": "10017-5703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States including Puerto Rico",
      "recall_number": "D-1446-2020",
      "product_description": "Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL) 2 mL Single-dose Fliptop Vials, Rx only, Distributed by Hospira, Inc. Lake Forest, IL 60045 USA  NDC 0409-9094-12",
      "product_quantity": "19,144 vials",
      "reason_for_recall": "Lack of Assurance of Sterility; potential loose metal overseal crimp defects.",
      "recall_initiation_date": "20200720",
      "center_classification_date": "20200804",
      "termination_date": "20221208",
      "report_date": "20200812",
      "code_info": "Lots: Tray lot: 13405DK Vial lot: 13-405 DK Exp. 1JUL2021, Tray lot: 17096DK Vial lot: 17-096-DK Exp. 1NOV2021",
      "more_code_info": ""
    }
  ]
}