{
  "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": [
    {
      "country": "United States",
      "city": "Oyster Bay",
      "address_1": "21 Singworth St",
      "reason_for_recall": "The device is used as part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits and may collapse during use which can increase resistance to flow in the venous line and cause a drop in circuit blood flow.",
      "address_2": "",
      "product_quantity": "147 units",
      "code_info": "Lot Number: 5290-201001  UDI: (01)00851997007004(10)5290-201001(17)20231021(11)20201021",
      "center_classification_date": "20210615",
      "distribution_pattern": "US Nationwide distribution in the states of AL, AR, CA, DC, FL, GA, IN, MO, NC, PA, SC, TX.",
      "state": "NY",
      "product_description": "The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits.   Model: BB14",
      "report_date": "20210623",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Circulatory Technology Inc.",
      "recall_number": "Z-1862-2021",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "88000",
      "more_code_info": "",
      "recall_initiation_date": "20210427",
      "postal_code": "11771-3703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}