{
  "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": "Bothell",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88637",
      "recalling_firm": "Philips North America LLC",
      "address_1": "22100 Bothell Everett Hwy",
      "address_2": "N/A",
      "postal_code": "98021-8431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, CT, FL, GA, IN, MI, MO, NJ, NY, OH, TX, and WA.  International distribution in the countries of Australia, Canada, France, Germany, Japan, Norway, Switzerland.",
      "recall_number": "Z-0081-2022",
      "product_description": "Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A",
      "product_quantity": "15 units",
      "reason_for_recall": "Customers were not notified of previous recalls associated with various defibrillator models.",
      "recall_initiation_date": "20210209",
      "center_classification_date": "20211008",
      "report_date": "20211020",
      "code_info": "Affected serial numbers for Model #  M5066A: A11K-03264, A07A-01278, B07F-01268, A10G-05443, A06E-00929, A06L-01867, A06L-01678, A07J-05837, A10C-03623, M5066A-ABD, A07K-02685, A09H-03908,  0205142344,  Expansion - additional serial numbers for Model # M5066A: A11K-08837,  Affected Serial numbers for Model # M5067A: A06K-02421."
    }
  ]
}