{
  "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": "Orlando",
      "address_1": "6700 Conroy Windermere Rd",
      "reason_for_recall": "Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes",
      "address_2": "Suite 140",
      "product_quantity": "5",
      "code_info": "B5008 exp 12/31/13, K5030 Exp. 11/30/13, A5716 Exp. 8/31/13, C5121 Exp 9/12/13, and C5208 Exp 9/7/13",
      "center_classification_date": "20130711",
      "distribution_pattern": "Nationwide and PR",
      "state": "FL",
      "product_description": "Alprostadil 2000 mcg/ml, compounded by Olympia Pharmacy, Orlando, FL",
      "report_date": "20130717",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Lowlite Investments, Inc. D/B/A Olympia Pharmacy",
      "recall_number": "D-695-2013",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Drugs",
      "event_id": "65360",
      "recall_initiation_date": "20130529",
      "postal_code": "32835-3500",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}