{
  "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": "Sandpoint",
      "state": "ID",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93648",
      "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: RI, CA, TX",
      "recall_number": "Z-0693-2024",
      "product_description": "Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)",
      "product_quantity": "195",
      "reason_for_recall": "Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.",
      "recall_initiation_date": "20230328",
      "center_classification_date": "20240117",
      "report_date": "20240124",
      "code_info": "UDI-DI: 00849436000693, Lots/Expiration: WO03739/September 13, 2024, and WO04218/November 14, 2024."
    }
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}