{
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    "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": [
    {
      "status": "Terminated",
      "city": "La Habra",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82483",
      "recalling_firm": "Auro Pharmacies Inc. DBA Central Drugs",
      "address_1": "511 S Harbor Blvd Ste F",
      "address_2": "N/A",
      "postal_code": "90631-9375",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-1082-2019",
      "product_description": "Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.",
      "product_quantity": "167 vials",
      "reason_for_recall": "Failed pH Specification: product does not meet pH label claim.",
      "recall_initiation_date": "20190322",
      "center_classification_date": "20190405",
      "termination_date": "20200227",
      "report_date": "20190417",
      "code_info": "Lot 190205@1, expiry 08/4/19"
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