{
  "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": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "79253",
      "recalling_firm": "Fagron, Inc",
      "address_1": "2400 Pilot Knob Rd",
      "address_2": "N/A",
      "postal_code": "55120-1118",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, USA",
      "recall_number": "D-0547-2018",
      "product_description": "SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by Fagron Inc. St. Paul, MN 55120",
      "product_quantity": "a) 1007 bottles (500 mL) and b) 738 bottles (4 L)",
      "reason_for_recall": "Microbial contamination of Non-Sterile Product;  product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).",
      "recall_initiation_date": "20180214",
      "center_classification_date": "20180227",
      "termination_date": "20190910",
      "report_date": "20180307",
      "code_info": "a) 17I28-U80-039976, exp. 10/02/2020; b) 17I28-U80-039977, exp. 10/02/2020"
    }
  ]
}