{
  "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": "95239",
      "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: Nationwide  OUS: Israel Japan Russia Switzerland Canada Turkey",
      "recall_number": "Z-3207-2024",
      "product_description": "Percussionaire, Inc., REF: P5-TEE,  Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve",
      "product_quantity": "50,460 units",
      "reason_for_recall": "Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.",
      "recall_initiation_date": "20240821",
      "center_classification_date": "20240927",
      "report_date": "20241009",
      "code_info": "No UDI/ Lots: 240620, 240610, 240418, 240326, 230612, WO07066, WO07010, WO06020, WO05019, WO04884, WO04827, WO04756, WO04714, WO04656, WO04625, WO04596, WO04553, WO04398, WO04356, WO04061, WO03846, WO03748, WO03688"
    }
  ]
}