{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Palm Beach Gardens",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69974",
      "recalling_firm": "The Anspach Effort, Inc.",
      "address_1": "4500 Riverside Dr",
      "address_2": "N/A",
      "postal_code": "33410-4235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CO, FL, LA, ID, CA, KS, IL, TX, VA, MI, NC, WA, AR, NY, NC, AZ, and Hawaii     Canada, Hong Kong, Chile, Israel, Poland, Turkey, Itly, Malaysia, Ireland, Korea, Germany, Spain, Norway, Sweeden, England, Fiji, Switzerland, Belgium, Austria, Netherlands, France, Japan, China, India, Thailand, Russia, Zaire, Taiwan, and Australia.",
      "recall_number": "Z-1017-2016",
      "product_description": "Synthes Small Electric Drive (SED)",
      "product_quantity": "302 (23 in the USA and 279 OUS)",
      "reason_for_recall": "May operate solely in reverse mode, not operate in reverse mode when intended, not function or an unintentionally start.",
      "recall_initiation_date": "20141114",
      "center_classification_date": "20160225",
      "report_date": "20160302",
      "code_info": "All lots from production launch",
      "more_code_info": ""
    }
  ]
}