{
  "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": "Murrysville",
      "address_1": "1001 Murry Ridge Ln",
      "reason_for_recall": "The polyester-based polyurethane (PE-PUR) foam may degrade into particles which may enter the devices air pathway and be ingested or inhaled by the user, and the PE-PUR foam may off-gas certain chemicals.",
      "address_2": "",
      "product_quantity": "8047",
      "code_info": "All Devices manufactured before 26 April 2021, All device serial numbers.    Material Numbers 1111181  1111182  1111178  1140184  1135427  1143671",
      "center_classification_date": "20210715",
      "distribution_pattern": "Worldwide distribution including US Nationwide, Argentina, Australia, Brazil, Canada, China, France, Germany, Italy, Japan, Korea, and Latin America.",
      "state": "PA",
      "product_description": "A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minimum Ventilatory Support, Facility Use",
      "report_date": "20210721",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Philips Respironics, Inc.",
      "recall_number": "Z-1957-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88071",
      "more_code_info": "",
      "recall_initiation_date": "20210614",
      "postal_code": "15668-8517",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}