{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69568",
      "recalling_firm": "Philips Medical Systems, Inc.",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to: Canada, Australia, Austria, Belgium, France, Germany, Iceland, Ireland, Italy, Japan, Kuwait, Netherlands, New Zealand, Norway, Portugal, Reunion, Romania, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Thailand, and the United Kingdom.",
      "recall_number": "Z-0206-2015",
      "product_description": "Gel-E Donut :  92025-A (Extra Small), 92025-B (Small),   92025-C (Medium)  and Squishon 2 91033-2.  The products are intended to support and cradle a baby's head and/or body.",
      "product_quantity": "336,695 units",
      "reason_for_recall": "Mold  on gel filled Gel-E and Squishon products",
      "recall_initiation_date": "20141010",
      "center_classification_date": "20141121",
      "termination_date": "20161129",
      "report_date": "20141203",
      "code_info": "All lot codes",
      "more_code_info": ""
    }
  ]
}