{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "1304 S Loop W",
      "reason_for_recall": "Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.",
      "address_2": "",
      "product_quantity": "85 vials",
      "code_info": "Lot: 10292018:21 Exp. 3/31/2019",
      "center_classification_date": "20181220",
      "distribution_pattern": "WA",
      "state": "TX",
      "product_description": "Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 --- NDC: 69699-1738-10",
      "report_date": "20181226",
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      "openfda": {},
      "recalling_firm": "Pharm D Solutions, LLC",
      "recall_number": "D-0343-2019",
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      "product_type": "Drugs",
      "event_id": "81629",
      "termination_date": "20201013",
      "more_code_info": "",
      "recall_initiation_date": "20181119",
      "postal_code": "77054-4010",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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