{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Romulus",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76318",
      "recalling_firm": "Metrex Research, LLC.",
      "address_1": "28210 Wick Rd",
      "address_2": "N/A",
      "postal_code": "48174-2639",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to PA, FL, IL, MN, TX, AL, NY",
      "recall_number": "Z-1402-2017",
      "product_description": "CaviWipes1 Extra Large, Part No. 13-5150  The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant. The device has been assigned the product code LRJ (General Purpose Disinfectant) by the FDA and is classified as a Class I Medical Device. CaviWipes1 Extra Large is intended to be used to disinfect surfaces.",
      "product_quantity": "960 cases",
      "reason_for_recall": "Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.",
      "recall_initiation_date": "20170120",
      "center_classification_date": "20170303",
      "termination_date": "20170901",
      "report_date": "20170315",
      "code_info": "Lot No. 16-2340PA"
    }
  ]
}