{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sandpoint",
      "state": "ID",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93476",
      "recalling_firm": "Percussionaire Corporation",
      "address_1": "130 Mcghee Rd Ste 109",
      "address_2": "N/A",
      "postal_code": "83864-8409",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:AL\tAR\tCA\tCT\tFL\tGA\tIL\tIN\tKS\tLA\tMI\tMN\tMO\tNC\tNJ\tOH\tOR\tTN\tTX\tUT\tVA OUS: None",
      "recall_number": "Z-0637-2024",
      "product_description": "High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123",
      "product_quantity": "2145 units",
      "reason_for_recall": "Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe  impact to the end user",
      "recall_initiation_date": "20231212",
      "center_classification_date": "20240117",
      "report_date": "20240124",
      "code_info": "UDI: (01)10849436000331/Lot # WO05216, WO05254, WO05321, WO05392, WO05559, WO05588, WO05684, WO05749, WO05896, WO05930,WO06028"
    }
  ]
}