{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lakewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89707",
      "recalling_firm": "Sensory Medical Inc",
      "address_1": "3333 S Wadsworth Blvd Unit D321",
      "address_2": "N/A",
      "postal_code": "80227-5142",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S. Nationwide distribution to states including: AK, AZ, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA. MD, MI, MN, MO. MS. NC, ND, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, and WI; and O.U.S Internationally to: Canada",
      "recall_number": "Z-0918-2022",
      "product_description": "Cub 2 Enclosed Bed Canopy System",
      "product_quantity": "225 devices",
      "reason_for_recall": "Due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.",
      "recall_initiation_date": "20220314",
      "center_classification_date": "20220414",
      "report_date": "20220420",
      "code_info": "Model/Product Code - Cub2 UDI Code: None Serial Numbers: All device manufactured/distributed prior to 12/16/2021."
    }
  ]
}