{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Jiutepec",
      "state": "N/A",
      "country": "Mexico",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78034",
      "recalling_firm": "Degasa Sa De Cv",
      "address_1": "Calle Centenario 15",
      "address_2": "Col. DEPORTIVA",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, IL.",
      "recall_number": "D-1129-2017",
      "product_description": "Povidone Iodine, USP Prep Solution, 10%, packaged in 1 gallon bottle, OTC, Manufactured for PSS World Medical, Inc. Southpoint Blvd. Jacksonville, FL  Made in Mexico, NDC 68345-350-09",
      "product_quantity": "720 bottles",
      "reason_for_recall": "Labeling: Label mix-up. Finished product Povidone iodine 7.5% was labeled as Povidone iodine 10% , the outer box had the correct label.",
      "recall_initiation_date": "20170804",
      "center_classification_date": "20170907",
      "termination_date": "20201124",
      "report_date": "20170913",
      "code_info": "Lot #: 3A176011, Exp 10/18"
    }
  ]
}