{
  "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": "255810",
      "code_info": "All Devices manufactured before 26 April 2021, All device serial numbers.    Material Numbers 1040001  1054096  1054097  1054260  1054655  1058180  1119867  1040001B  1054096B  1054096NB  1054097B  1054260B  1054655B  1054655TP  1054655TPV  1058180B  AU1054096  AU1054096B  BR1054096  BT1054096  BT1054260  CA1054096  CA1054096B  CN1054096  IT1054096B  KO1054096  KR1054096  LA1054096  LG1054096  R1054096  R1054096B  R1054097  R1054097B  R1054260  R1054260B  R1054655  R1054655B  R1054655TP  R1054655TPV  R1119867  RSL1054260  RSL1054260B  RTO1054260  RTO1054260B  U1054096  U1054096B  U1054097  U1054097B  U1054260  U1054260B  U1054655  RBR1054096  RTO1119867  1032800  1032802  1032804  1040002  1040005  1032800B  1032802B  1032804B  1032804TP  1032804TPV  1040002B  1040005B  1125564B  AU1032800  AU1032800B  BR1032800  CA1032800  CA1032800B  IT1032800B  KO1032800  KR1032800  LA1032800  LG1032800  R1032800  R1032802  R1032804  R1032804B  R1032804TP  R1032804TPV  R1040005  R1040005B  RTO1040005B  SP1032800B  U1032800  U1032802  U1032804  U1040005  U1040005B",
      "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": "Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.",
      "report_date": "20210721",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Philips Respironics, Inc.",
      "recall_number": "Z-1956-2021",
      "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"
    }
  ]
}