{
  "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 to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets",
      "address_2": "",
      "product_quantity": "99/500 mg tablets",
      "code_info": "Use by 12/14/2012, Lot# 002B90, NDC 16714-586-01",
      "center_classification_date": "20140723",
      "distribution_pattern": "Product was shipped to the following states: CO, MA, OH, TX & WY.",
      "state": "OH",
      "product_description": "Pramipexole Dihydrochloride Tablets, 0.5 mg, Rx, packaged and labeled to contain Nebivolol tablets, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Northstar Rx, Memphis, TN   NDC 16714-586-01",
      "report_date": "20140730",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Shamrock Medical Solutions Group LLC",
      "recall_number": "D-1449-2014",
      "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"
    }
  ]
}