{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Carlsbad",
      "address_1": "2885 Loker Ave E",
      "reason_for_recall": "The recall was initiated because Breg has determined that some Sterile Polar Pads products manufactured from January 2010 to October 2012 may have sustained damage to the product packaging which may compromise product sterility assurance.",
      "address_2": "",
      "product_quantity": "44,883 units",
      "code_info": "Affected product will be identified by date of manufacture from January 2010 through October 2012",
      "center_classification_date": "20130212",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Australia, Singapore, Chile, Latvia.",
      "state": "CA",
      "product_description": "BREG Sterile Polar Pads; 02356 Rev M, PAD M/U XL STER, Mfg.Date: 112012. Model #s: 02510, 09901, 02330, 02350, 02490, 02356, 02496, 02410, 02430. Local anesthetic effect.",
      "report_date": "20130220",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Breg Inc",
      "recall_number": "Z-0804-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64177",
      "termination_date": "20130701",
      "more_code_info": "",
      "recall_initiation_date": "20130114",
      "postal_code": "92010-6626",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}