{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Kalona",
      "address_1": "102 1st St S",
      "reason_for_recall": "Scales adhered to the product may be misaligned from the zero reference such that one side will not match the other.",
      "address_2": "",
      "product_quantity": "138 belly boards",
      "code_info": "Lot #'s: M441670, M469970, M469980, M469990, M484910, M484920, M516200, M516210, M516220, M533340, M533350, M533360, M533370, M533380, M533970, M533980, M533990, M534000, M544650, M544660, M544670, M550150, M551490, M554940, M554950, M556540, M556550, M559560, M560740, M575850, M578310, M581730, M591090, M591100, M591110, M591120, M591130, and M599570",
      "center_classification_date": "20140121",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS, MA, MD, MI, MN, MT, NC, NJ, NY, OH, OK, PA, SC, TN, TX, VA, WA, WI, and WV. Foreign distribution was made to Brazil, Canada, Chile, Czech Republic, France, Germany, Iraq, Israel, Italy, Japan, Malaysia, Saudi Arabia, Slovenia, South Korea, Spain, Turkey, and United Arab Emirates.",
      "state": "IA",
      "product_description": "Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, packaged 1 per box.     Product Usage:  This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Civco Medical Instruments Inc",
      "recall_number": "Z-0802-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66591",
      "termination_date": "20170202",
      "more_code_info": "",
      "recall_initiation_date": "20131025",
      "postal_code": "52247-9589",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}