{
  "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": "Shenandoah",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65154",
      "recalling_firm": "Lloyd Inc. of Iowa",
      "address_1": "604 W Thomas Ave",
      "address_2": "N/A",
      "postal_code": "51601-1744",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The firm distributed the bulk product to Forest Laboratories, Inc, St. Louis, MO who repackaged the product into 100-tablet bottles and distribution was made to 75 customers Nationwide and Puerto Rico.",
      "recall_number": "D-444-2013",
      "product_description": "Lloyd Thyro-Tab 0.200 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX.  The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.",
      "product_quantity": "5,771,989 tablets",
      "reason_for_recall": "cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.",
      "recall_initiation_date": "20130401",
      "center_classification_date": "20130521",
      "termination_date": "20140508",
      "report_date": "20130529",
      "code_info": "Lot #: HD29411, Exp May-13; HE00512, Exp Jul-13; HF062122, Exp Sep-13."
    }
  ]
}