{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91488",
      "recalling_firm": "Beaver Visitec International, Inc.",
      "address_1": "500 Totten Pond Rd",
      "address_2": "10 City Point",
      "postal_code": "02451-1916",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution in AL, CA, CO, DC, FL, GA, IL, LA, MD, MN, MT, NC, NH, NJ, NM, NY, OH OK, PA, RI, TN, TX, UT, VA, VT, WA, and WI  OUS distribution to Canada, Japan, and South Africa",
      "recall_number": "Z-1199-2023",
      "product_description": "Ultracell Wick with 80cc Collection Bag, 20/box",
      "product_quantity": "4640 units in total",
      "reason_for_recall": "Device packaging may contain open seals, compromising product sterility.",
      "recall_initiation_date": "20221220",
      "center_classification_date": "20230301",
      "report_date": "20230308",
      "code_info": "Catalog #40430, Lot Numbers 21M3820 and 21L3403  UDI/DI: 30886158012123",
      "more_code_info": ""
    }
  ]
}