{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Ocean",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99811",
      "recalling_firm": "Limitless Cryo Spa LLC",
      "address_1": "21 High Ridge Rd",
      "address_2": "N/A",
      "postal_code": "07712-3460",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0080-2027",
      "product_description": "Glypto Device, Glypto Cryo Machine;",
      "product_quantity": "219",
      "reason_for_recall": "Lack of 510(k) clearance.",
      "recall_initiation_date": "20260824",
      "center_classification_date": "20261002",
      "report_date": "20261014",
      "code_info": "All Glypto units distributed, placed, held, loaned, inventoried, or otherwise supplied by/through Limitless through the 08/11/2026 operational hold; 08/20/2026 preliminary field notice. Serial/account-specific consignee list attached or to be supplemented."
    }
  ]
}