{
  "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": "Weston",
      "address_1": "2400 N Commerce Pkwy Ste 400",
      "reason_for_recall": "Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.",
      "address_2": "",
      "product_quantity": "1,749 Bottles",
      "code_info": "Lot: 7212558, Exp 12/12.",
      "center_classification_date": "20120807",
      "distribution_pattern": "Nationwide",
      "state": "FL",
      "product_description": "Meloxicam Tablets, USP, 15 mg, Rx Only, 100 Tablets per Bottle, Manufactured by: Strides Acrolab Ltd., Bangalore-560 076, India, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-3579-1.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Apotex Corp.",
      "recall_number": "D-1443-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "62436",
      "termination_date": "20130919",
      "more_code_info": "",
      "recall_initiation_date": "20120405",
      "postal_code": "33326-3253",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}