{
  "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": "Chesapeake",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "91466",
      "recalling_firm": "Sentara Infusion Services",
      "address_1": "535 Independence Pkwy Ste 300",
      "address_2": "N/A",
      "postal_code": "23320-5176",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Dispensed to Patients Nationwide.",
      "recall_number": "D-0324-2023",
      "product_description": "VITAMIN K(PHYTONADIONE) 2.5MG(0.25ML) SYRINGE, Rx only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,",
      "product_quantity": "1 bag",
      "reason_for_recall": "Lack of sterility assurance",
      "recall_initiation_date": "20221227",
      "center_classification_date": "20230215",
      "termination_date": "20260220",
      "report_date": "20230222",
      "code_info": "Beyond Use DateL December 29, 2022"
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}