{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Charlotte",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82620",
      "recalling_firm": "CMC Enterprise Pharmacy",
      "address_1": "4400 Golf Acres Dr",
      "address_2": "N/A",
      "postal_code": "28208-5968",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NC",
      "recall_number": "D-1240-2019",
      "product_description": "DelNido Cardioplegia (Normosol-R pH 7.4 or Plasma-Lyte A pH 7.4 1000 mL bag) Mannitol 20%-16.3 mL, Potassium Chloride 2 meq/mL-13 mL, Sodium Bicarbonate 8.4%-Lidocaine 1%-1:1 Dilution-26 mL, Magnesium Sulfate 500 mg/mL-4 mL, Cardiac Perfusion Only - Not for IV Use, Made by: Enterprise Pharmacy, 4400 Golf Acres Drive, Bldg. J Suite E, Charlotte, NC, 28208.",
      "product_quantity": "110 bags",
      "reason_for_recall": "Lack of sterility assurance.",
      "recall_initiation_date": "20190412",
      "center_classification_date": "20190423",
      "termination_date": "20191030",
      "report_date": "20190501",
      "code_info": "Lots: ED041909 Exp. 4/13/2019; ED111907 Exp. 4/20/2019"
    }
  ]
}