{
  "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": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Completed",
      "city": "Columbia",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92754",
      "recalling_firm": "The Ritedose Corporation",
      "address_1": "1 Technology Cir",
      "address_2": "N/A",
      "postal_code": "29203-9591",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide in the US",
      "recall_number": "D-0946-2023",
      "product_description": "Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC 29203, NDC 76204-025-96.",
      "product_quantity": "44 cartons",
      "reason_for_recall": "CGMP deviation: product released prior to supplier approval.",
      "recall_initiation_date": "20230721",
      "center_classification_date": "20230731",
      "report_date": "20230809",
      "code_info": "Lot: 23CE2, Exp. 03/31/2026"
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}