{
  "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": "Staten Island",
      "address_1": "119 Linwood Ave",
      "reason_for_recall": "Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.",
      "address_2": "",
      "product_quantity": "unknown",
      "code_info": "All Lots",
      "center_classification_date": "20180228",
      "distribution_pattern": "NY and NJ through six retail stores named \"Asian Food Markets\"",
      "state": "NY",
      "product_description": "Ye Lang Shen capsules, 5000 mg, 8-count bottle, labeling is in foreign language",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "A&H Focal Inc.",
      "recall_number": "D-0561-2018",
      "initial_firm_notification": "Press Release",
      "product_type": "Drugs",
      "event_id": "76644",
      "termination_date": "20190614",
      "more_code_info": "",
      "recall_initiation_date": "20170307",
      "postal_code": "10305-4445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}