{
  "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": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92253",
      "recalling_firm": "Central Admixture Pharmacy Services, Inc.",
      "address_1": "6580 Snowdrift Rd Ste 100",
      "address_2": "N/A",
      "postal_code": "18106-9331",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-0652-2023",
      "product_description": "Cardioplegia Solution, Reperfusate 4:1 low potassium, 7.5 mEq K, packaged in 238.75 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA  18106, NDC 71285-0007-1.",
      "product_quantity": "140 bags",
      "reason_for_recall": "Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.",
      "recall_initiation_date": "20230428",
      "center_classification_date": "20230519",
      "termination_date": "20250622",
      "report_date": "20230531",
      "code_info": "Lot # 37-896489, Exp 05/07/2023; 37-897805, Exp 05/12/2023; 37-900959, Exp 05/26/2023"
    }
  ]
}