{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "73858",
      "product_res_number": "Z-0201-2009",
      "event_date_initiated": "2008-10-01",
      "event_date_posted": "2008-11-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-05-21",
      "res_event_number": "49590",
      "product_description": "Vibe Technologies, VIBE machine, Vibrational Integrated Biophotonic Energizer.",
      "code_info": "All serial numbers",
      "firm_fei_number": "3004494240",
      "recalling_firm": "VIBE Technologies",
      "address_1": "2329 W 10th St",
      "city": "Greeley",
      "state": "CO",
      "postal_code": "80634-3527",
      "additional_info_contact": "Gene Koonce\n970-356-9594",
      "reason_for_recall": "Medical device marketed without marketing approval for claims that include cures cancer, infections, depression.",
      "root_cause_description": "PMA",
      "action": "Vibe Technologies notified their customers by letter on October 1, 2008 and were told to discontinue use as a medical device.  This letter notification included: \n\n1.  A warning label to be placed on the Vibe machine stating that it is not a medical device and should not be used as such.\n\n2.  An updated operation manual/users guide containing no medical conditions or human body claims.\n\n3.  A certification to be signed by the user and returned acknowledging that they: received the letter; affixed the warning label to the Vibe machine; understand that the Vibe machine does not affect the structure/function of the human or animal body; will not promote the Vibe machine as a medical device; will remove any medical claims from their website; destroy any Vibe literature making medical claims.  Approximately three weeks after the certified mailing, the firm will begin performing recall effectiveness checks.",
      "product_quantity": "851 units",
      "distribution_pattern": "Worldwide",
      "openfda": {}
    }
  ]
}