{
  "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": [
    {
      "country": "United States",
      "city": "Tulsa",
      "address_1": "12515 E 55th St Ste 100",
      "reason_for_recall": "Tablet Separation: The manufacturer of Arthrotec had recalled the lots that were used to re-package this product because they may contain broken tablets.",
      "address_2": "",
      "product_quantity": "a) 4 bottles; b) 2 bottles",
      "code_info": "Lot #: a) 5NON, Exp 04/13; 5YUN, Exp 09/13; b) 5KBJ, Exp 02/13; 5LVX, Exp 04/13",
      "center_classification_date": "20120614",
      "distribution_pattern": "NC and KY",
      "state": "OK",
      "product_description": "Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 30-count tablets per bottle (NDC 54868-4165-1); b) 60-count tablets per bottle (NDC 54868-4165-0); Rx only, Mfg. By: G.D. searle LLC Div Pfizer, New York, NY  10017; Repacked & distributed by: Physicians total Care, Inc., Tulsa, OK  74146.",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Physicians Total Care, Inc.",
      "recall_number": "D-1379-2012",
      "initial_firm_notification": "FAX",
      "product_type": "Drugs",
      "event_id": "62135",
      "termination_date": "20130222",
      "more_code_info": "",
      "recall_initiation_date": "20110919",
      "postal_code": "74146-6234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}