{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "6225 Progressive Dr",
      "reason_for_recall": "Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading because they may be confused with Pentrexyl, a prescription antibiotic used to treat respiratory illnesses in Mexico.",
      "address_2": "# 200",
      "product_quantity": "11,580 cartons",
      "code_info": "Lot #: 11611B0, Batch # 114039, Exp 10/14",
      "center_classification_date": "20130425",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Pentrexcilina (acetaminophen, chlorpheniramine maleate, and phenylephrine HCl) tablets, 20-count tablets per carton, Distributed by: Laboratorios Norimex Co., San Diego, CA  92154, UPC 0 91965 02002 8.",
      "report_date": "20130501",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "OPMX, LLC",
      "recall_number": "D-299-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "64933",
      "termination_date": "20130822",
      "more_code_info": "",
      "recall_initiation_date": "20130412",
      "postal_code": "92154-6643",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}