{
  "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": [
    {
      "country": "United States",
      "city": "Federal Way",
      "address_1": "530 S 336th St",
      "reason_for_recall": "Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.",
      "address_2": "",
      "product_quantity": "5 vials total (2/5 mL vials, 1/10mL vial, and 2/15mL vials)",
      "code_info": "Lot # t01-05-2017@102, Exp 7/5/2017; t02-02-2017@105, Exp 8/2/2017; t02-10-2017@121, Exp 8/2/2017.",
      "center_classification_date": "20170517",
      "distribution_pattern": "Distributed nationwide in U.S.A.,  Australia and Canada.",
      "state": "WA",
      "product_description": "PGE1 MDV 20MCG/ML INJ, Injection, 20mcg/mL, Rx only, packaged in a 5 mL, 10mL, and 15 mL Glass/Multiple Dose vials, Prepared by Key Compounding Pharmacy",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Key Pharmacy and Compounding Center",
      "recall_number": "D-0731-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "76912",
      "termination_date": "20170829",
      "more_code_info": "",
      "recall_initiation_date": "20170418",
      "postal_code": "98003-6383",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}