{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA087242"
        ],
        "brand_name": [
          "AMINOPHYLLINE"
        ],
        "generic_name": [
          "AMINOPHYLLINE"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-5921",
          "0409-5922"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "AMINOPHYLLINE DIHYDRATE"
        ],
        "rxcui": [
          "1724666",
          "1724668"
        ],
        "spl_id": [
          "a36bc745-4366-4883-8e7d-4df241a069c4"
        ],
        "spl_set_id": [
          "9a663ef3-881f-48bd-2689-3713b24545c2"
        ],
        "package_ndc": [
          "0409-5921-16",
          "0409-5921-01",
          "0409-5922-16",
          "0409-5922-01"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "C229N9DX94"
        ]
      },
      "product_type": "Drugs",
      "event_id": "90903",
      "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": "Distributed in the United States and Puerto Rico.",
      "recall_number": "D-0003-2023",
      "product_description": "Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only,  Distributed by Hospira, Inc. Lake Forest, IL 60045 USA. NDC 0409-5921-16 (vial) 0409-5921-01 (carton)",
      "product_quantity": "103,150 10 mL vials",
      "reason_for_recall": "Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial.",
      "recall_initiation_date": "20220927",
      "center_classification_date": "20221004",
      "termination_date": "20240821",
      "report_date": "20221012",
      "code_info": "Lot: 30-137-DK Exp. 1 DEC. 2022"
    }
  ]
}