{
  "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": "72665",
      "code_info": "All Devices manufactured before 26 April 2021, All device serial numbers.    Material Numbers 1076492  1076493  1076495  1076538  1076539  1076565  1076566  1076579  1076580  1076583  1076584  1076586  1078226  1078297  1104171  1111168  1111169  1111170  1111171  1111172  1111173  1111174  1111175  1111176  1111177  1116156  1122129  1140798  1140799  1111170S  1111170-S  AR1111169  BR1076493  BR1076566  BR1111169  CN1076493  CN1076566  CN1111169  GB-SPK0011  GB-SPK0012  IT1111169  LA1076493  LA1076566  R1076495  R1111169  R1111177  R1116156  1104170  R1111175  RBR1111169  U1116156  1038916  1038917  1040716  1044114  1044235  1038987  1040717  1068942  1068943  1042900  1042901  1042903  1042904  1042906  1042907  1044288  1044289  1040718  1067255  1029744  1029750  1029756  1029757  1029758  1029759  AU1029756  CA1029756  CA1029759  LA1029756  1030075  1055770  1055813",
      "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 A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting",
      "report_date": "20210721",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Philips Respironics, Inc.",
      "recall_number": "Z-1958-2021",
      "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"
    }
  ]
}