{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Greenwood Village",
      "address_1": "6000 Greenwood Plaza Blvd",
      "reason_for_recall": "Incorrect Power Supply in the package, rendering the device inoperable.",
      "address_2": "Ste 110",
      "product_quantity": "32 units",
      "code_info": "Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052",
      "center_classification_date": "20160427",
      "distribution_pattern": "Distributed to 1 consignee located in the United States.",
      "state": "CO",
      "product_description": "reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS)      Product Usage:  The reVive Light Therapy Pain Relief Device is a device designed to deliver LED light spectrum in 880nm and 660nm directly into the body tissue to increase circulation and temporarily relieve pain associated with muscle spasms, arthritis, general aches and strains.",
      "report_date": "20160504",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "LED Technologies, LLC",
      "recall_number": "Z-1581-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73779",
      "termination_date": "20161130",
      "recall_initiation_date": "20160330",
      "postal_code": "80111-4816",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}