{
  "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": [
    {
      "status": "Ongoing",
      "city": "Murrysville",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88333",
      "recalling_firm": "Philips Respironics, Inc.",
      "address_1": "1001 Murry Ridge Ln",
      "address_2": "N/A",
      "postal_code": "15668-8517",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US nationwide distribution.",
      "recall_number": "Z-2287-2021",
      "product_description": "Trilogy Evo, Product numbers BL2110X15B, CA2110X12B, DE2110X13B, DS2110X11B, EE2110X15B, ES2110X15B, EU2110X15B, EU2110X19, FR2110X14B, GB2110X15B, IA2110X15B, IN2110X15B, IN2110X19, IT2110X21B, KR2110X15B, LA2110X15B, LD2110X23B, ND2110X15B, RDE2110X13B, UDS2110X11B",
      "product_quantity": "18588 (US); 5662 (OUS)",
      "reason_for_recall": "Two software issues have been identified related to pressure increase in the device: The first issue is described as \"Infant/Pediatric EFS Calibration Pressure Increase\" and the second issue is described as \"Pressure Drift (Continuous Usage).",
      "recall_initiation_date": "20210726",
      "center_classification_date": "20210813",
      "report_date": "20210825",
      "code_info": "Software version numbers 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02"
    }
  ]
}