{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66509",
      "recalling_firm": "3M Company - Health Care Business",
      "address_1": "3M Center 2510 Conway Ave , B# 275-5-W-6",
      "address_2": "N/A",
      "postal_code": "55144",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including IN, TX, PA, FL, NV, SC, and TN and Internationally to Canada and Saudi Arabia.",
      "recall_number": "Z-0428-2014",
      "product_description": "3M ESPE, Unitek Stainless Steel Permanent Molar Crowns    Stainless Steel Crowns, are designed to fill the need for long term provisional coverage on adult molars and bicuspids as well as pediatric posterior and anterior teeth.",
      "product_quantity": "1419 (1325 US, 94 OUS)",
      "reason_for_recall": "3M  is recalling specific lots of 3M ESPE Unitek Primary Stainless Steel Crowns - Series UR4 contain LL3 crowns which are incorrectly labeled as UR4 crowns.",
      "recall_initiation_date": "20130605",
      "center_classification_date": "20131127",
      "termination_date": "20131211",
      "report_date": "20131204",
      "code_info": "Product Code 902150 (Kit)  ¿ Lot Codes N484233 and N463186  Product Code 900224 (Refill)  ¿ Lot Codes N466509 and N473723"
    }
  ]
}