{
  "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": [
    {
      "country": "United States",
      "city": "Dayton",
      "address_1": "36 Stults Rd",
      "reason_for_recall": "Lack of assurance of sterility: Three lots were released where there was a failure to follow proper testing and investigation procedures. Product may be out of specification (OOS) for endotoxin.",
      "address_2": "",
      "product_quantity": "24 Viaflex Bag",
      "code_info": "Lot #: 180040003D, Exp 3/18/18",
      "center_classification_date": "20180329",
      "distribution_pattern": "Product was distributed to SC, FL, NY, NY,WA",
      "state": "NJ",
      "product_description": "15 units Oxytocin added to 0.9% Sodium Chloride Injection, 250 mL Viaflex Bag, Rx only, PharMEDium Serivces, LLC",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "PharMEDium Services, LLC",
      "recall_number": "D-0422-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "79063",
      "termination_date": "20180424",
      "more_code_info": "",
      "recall_initiation_date": "20180205",
      "postal_code": "08810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}