{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
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        ],
        "brand_name": [
          "SODIUM BICARBONATE"
        ],
        "generic_name": [
          "SODIUM BICARBONATE"
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        "manufacturer_name": [
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        ],
        "product_ndc": [
          "0409-6637",
          "0409-4916"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
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        "substance_name": [
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        "rxcui": [
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          "792582"
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          "0409-4916-14",
          "0409-6637-24",
          "0409-6637-14"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "8MDF5V39QO"
        ]
      },
      "product_type": "Drugs",
      "event_id": "93681",
      "recalling_firm": "Pfizer Inc.",
      "address_1": "235 East 42nd Street",
      "address_2": "N/A",
      "postal_code": "10017-5703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA and Puerto Rico.",
      "recall_number": "D-0234-2024",
      "product_description": "8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).",
      "product_quantity": "21200 Cartons",
      "reason_for_recall": "Presence of Particulate Matter; identified as glass",
      "recall_initiation_date": "20231221",
      "center_classification_date": "20240117",
      "report_date": "20240124",
      "code_info": "Lot HA7295, EXP 03/01/2025"
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}