{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63692",
      "recalling_firm": "Stryker Sustainability Solutions",
      "address_1": "1810 W Drake Dr",
      "address_2": "N/A",
      "postal_code": "85283-4327",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in Arizona and New Jersey.",
      "recall_number": "Z-0840-2013",
      "product_description": "STRYKER Sustainability Solutions, AC Power Adaptor for Restep Deep Vein Thrombosis (DVT) System, an external compression system.  PUMPKIT (Pump Kit), and RSP159-01 (AC Power Adaptor).",
      "product_quantity": "1,311",
      "reason_for_recall": "Reports that the AC Power Adaptor may not operate due to wires coming loose in the unit.",
      "recall_initiation_date": "20120830",
      "center_classification_date": "20130220",
      "termination_date": "20140930",
      "report_date": "20130227",
      "code_info": "108851407, 108851408, 108870192, 108874144, 108883271, 108886340, and 108888023."
    }
  ]
}