{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Phoenix",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92707",
      "recalling_firm": "Central Admixture Pharmacy Services, Inc.",
      "address_1": "2200 S 43rd Ave",
      "address_2": "N/A",
      "postal_code": "85043-3909",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0990-2023",
      "product_description": "potassium phosphate, 30 mmole added to 0.9% sodium Chloride 500mL, IV Bag, RX Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-7016-1",
      "product_quantity": "234 bags",
      "reason_for_recall": "Lack of assurance of sterility. Validation data for decontamination cycles is lacking.",
      "recall_initiation_date": "20230714",
      "center_classification_date": "20230801",
      "termination_date": "20250328",
      "report_date": "20230809",
      "code_info": "Lot: 36-256240, Exp.9/12/2023."
    }
  ]
}