{
  "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": "Bridgewater",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "87093",
      "recalling_firm": "Bausch Health Companies, Inc.",
      "address_1": "400 Somerset Corporate Blvd",
      "address_2": "",
      "postal_code": "08807-2867",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed Nationwide in the USA",
      "recall_number": "D-0244-2021",
      "product_description": "Phytonadione Tablets 5mg, 30-count bottle, Rx Only, Manufactured For: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA NDC 68682-170-30",
      "product_quantity": "14,089 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.",
      "recall_initiation_date": "20210107",
      "center_classification_date": "20210125",
      "termination_date": "20220211",
      "report_date": "20210203",
      "code_info": "Lot: 18L091P, Exp 05/2021",
      "more_code_info": ""
    }
  ]
}