{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Glendora",
      "address_1": "1332 S Lone Hill Ave",
      "reason_for_recall": "Ormco Corporation is recalling Copper NiTi Preformed Archwires because the product transformation temperature as listed on the labeling is incorrect.",
      "address_2": "",
      "product_quantity": "161 units",
      "code_info": "Lot No. 21538339",
      "center_classification_date": "20151130",
      "distribution_pattern": "Distributed US (nationwide) and the countries of Canada, Japan, Mexico, Russia, and Peru.",
      "state": "CA",
      "product_description": "Copper NiTi Preformed Archwires; Copper NiTi 40 BAF .016X.022 LO Pk10, Part No. 211-0952.  Intended to provide tooth movement.",
      "report_date": "20151209",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ormco/Sybronendo",
      "recall_number": "Z-0343-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72590",
      "termination_date": "20160119",
      "more_code_info": "",
      "recall_initiation_date": "20151104",
      "postal_code": "91740-5339",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}