{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89805",
      "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 and Puerto Rico, Canada, Columbia, France",
      "recall_number": "D-0856-2022",
      "product_description": "SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only,  Manufactured for Fagron, Inc., St. Paul, MN 55120.",
      "product_quantity": "a) 559 bottles and b) 243 bottles",
      "reason_for_recall": "Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.",
      "recall_initiation_date": "20220304",
      "center_classification_date": "20220509",
      "report_date": "20220518",
      "code_info": "Lot #: a) A67185, Exp. Date 08/31/2024; b) Lot #: A67186, Exp. Date 08/31/2024"
    }
  ]
}