{
  "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": "Tulsa",
      "state": "OK",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67118",
      "recalling_firm": "Physicians Total Care, Inc.",
      "address_1": "12515 E 55th St Ste 100",
      "address_2": "N/A",
      "postal_code": "74146-6234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "FAX",
      "distribution_pattern": "CA, GA, NC, and MO",
      "recall_number": "D-390-2014",
      "product_description": "Carisoprodol IV ( Carisoprodol Tablets USP) 350mg, RX only.  Mfd by: Shasun Chemicals Drugs LTD, Pondicherry, INDIA. Repacked and Distributed by: Physicians Total Care, Inc., Tulsa, OK  74146.  90 count bottle: NDC: 54868-0816-8, 60 count bottle: NDC: 54868-0816-4, 30 count bottle: NDC: 54686-0816-3.",
      "product_quantity": "3,000 tablets",
      "reason_for_recall": "Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine stability testing.",
      "recall_initiation_date": "20131122",
      "center_classification_date": "20131226",
      "termination_date": "20160302",
      "report_date": "20140101",
      "code_info": "NDC 54868-0816-8, LOT: 6REE,  EXP. 8/14;   NDC 54868-0816-4, LOT: 6RED,  EXP. 8/14;   NDC 54868-0816-3, LOT: 6REB,  EXP. 8/14;",
      "more_code_info": ""
    }
  ]
}