{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "123693",
      "product_res_number": "Z-0464-2014",
      "event_date_initiated": "2013-10-28",
      "event_date_posted": "2013-12-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-01-29",
      "res_event_number": "66830",
      "product_code": "LDQ",
      "product_description": "Centurion Sterile # 84 Rubber Bands Reorder EB84,  Caution: This product contains natural rubber latex  which may cause allergic reactions.\n LATEX FREE ,   CAUTION: FEDERAL lAW (USA) RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN\nSingle Use Only\n\nbands items together and podiatry office uses bands as tourniquet on toe during in grown toenail procedure",
      "code_info": "EB84, Lot 2013041801 Expriation 2018/03",
      "firm_fei_number": "1824619",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "301 Catrell Dr",
      "city": "Howell",
      "state": "MI",
      "postal_code": "48843-1703",
      "additional_info_contact": "Matthew K. Price,\n517-546-5400",
      "reason_for_recall": "Package labeling indicates both \"latex free\"  and \"contains natural rubber latex\" . The rubber bands do contain natural rubber latex.   This could cause a significant risk to users with latex allergies.",
      "root_cause_description": "Labeling False and Misleading",
      "action": "Centurion sent a Urgent Recall Notification letter via Certified Mail October 31, 2013, return receipt to all affected customers. The affected Centurion Medical Products Corporation sales representatives were notified via email on October 28, 2013.  \n\nCustomers were instructed to destroy all implicated product and  complete the accountability record included with the notice and fax to 517-546-3356.  Customers were asked to forward a copy of the notice if product was further distributed.   Additional notices will be mailed to non-responsive customers via Certified Mail Return\nReceipt, and will be documented in the recall file.  For further questions please call (517) 546-5400.",
      "product_quantity": "500 lots",
      "distribution_pattern": "US Distribution including the states of GA, LA and NY.",
      "openfda": {
        "k_number": [
          "K802042",
          "K760052",
          "K945374",
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          "1423537",
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          "9616088",
          "3008061617",
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          "9610849",
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        ],
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          "1000512168",
          "3004167615",
          "3008061617",
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          "3002807170",
          "3002902735",
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}