{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mundelein",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72323",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "1 Medline Pl",
      "address_2": "",
      "postal_code": "60060-4485",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0662-2016",
      "product_description": "ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets, 500 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-641-30.",
      "product_quantity": "7,372 HDPE Bottles",
      "reason_for_recall": "Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.",
      "recall_initiation_date": "20150925",
      "center_classification_date": "20160212",
      "termination_date": "20160629",
      "report_date": "20160224",
      "code_info": "lot # 45810; Exp. 05/18",
      "more_code_info": ""
    }
  ]
}