{
  "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": "Lewis Center",
      "address_1": "741 Radio Dr",
      "reason_for_recall": "Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL",
      "address_2": "",
      "product_quantity": "55/1 mL/20mg/mL syringe",
      "code_info": "Lot #: 002HZI Use By: 7/20/2013 NDC: 00527-1426-36",
      "center_classification_date": "20140723",
      "distribution_pattern": "Product was shipped to the following states: CO, MA, OH, TX & WY.",
      "state": "OH",
      "product_description": "Oxycodone HCl Oral Concentrate, 20 mg/mL, Rx (C-II) Packaged and labeled as Morphine Sulfate 20 mg/mL, Mfg: Lannett Co. Inc., Re-Packaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfr: Cody Laboratories Inc., Cody, WY  NDC 00527-1426-36",
      "report_date": "20140730",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Shamrock Medical Solutions Group LLC",
      "recall_number": "D-1447-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "64611",
      "termination_date": "20140731",
      "more_code_info": "",
      "recall_initiation_date": "20110927",
      "postal_code": "43035-7134",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}