{
  "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-0078-2022",
      "product_description": "Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A",
      "product_quantity": "4 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": "Model M3860A affected serial numbers: A09G-04198 and 510800626 Model M3861A affected serial numbers: A09H-00436 and A07J-03514"
    }
  ]
}