{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Middleburg Heights",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91923",
      "recalling_firm": "Compass Health Brands (Corporate Office)",
      "address_1": "6753 Engle Rd",
      "address_2": "N/A",
      "postal_code": "44130-7934",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-1398-2023",
      "product_description": "REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas.    Models: DVTREX-U and DVTREX -L",
      "product_quantity": "30 units",
      "reason_for_recall": "Error in the Introduction section of the user manual that indicates the device may be used for the prevention of deep vein thrombosis (DVT). Marketed without a 510k for this indication",
      "recall_initiation_date": "20230307",
      "center_classification_date": "20230418",
      "report_date": "20230426",
      "code_info": "UDI-DI: DVTREX-L: 00092237622933  DVTREX-U: 00092237622926   All Serial Numbers"
    }
  ]
}