{
  "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": [
    {
      "status": "Terminated",
      "city": "Carlsbad",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "58247",
      "recalling_firm": "Breg Inc, An Orthofix Company",
      "address_1": "2885 Loker Ave E",
      "address_2": "N/A",
      "postal_code": "92010-6626",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) and country of: Nova Scotia.",
      "recall_number": "Z-2326-2012",
      "product_description": "Polar Dressing, Knee/MU/Shldr Intelli-Flo-Breg, PN 10630    Used with cold therapy pads to provide insulation barrier between the pad and patient's skin.",
      "product_quantity": "502 units",
      "reason_for_recall": "This recall has been initiated due to confirmation that the Polar Dressing, Knee/MU/Shldr Intelli-Flo-Breg does not meet the required thickness as specified. The dressing in the sterile pouch measures a thickness of 0.010\" instead of 0.020\". This change in thickness makes the dressing  thinner, less durable and subject to tearing. The product is mislabeled.",
      "recall_initiation_date": "20100811",
      "center_classification_date": "20120906",
      "termination_date": "20120906",
      "report_date": "20120912",
      "code_info": "Lot # D101564"
    }
  ]
}