{
  "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": "Terminated",
      "city": "Palm Beach Gardens",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63086",
      "recalling_firm": "The Anspach Effort, Inc.",
      "address_1": "4500 Riverside Drive",
      "address_2": "N/A",
      "postal_code": "33410-4235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and the countries of: Italy, Japan, Switzerland, Turkey and Taiwan.",
      "recall_number": "Z-0076-2013",
      "product_description": "\"***Electric Systems Foot Control with Direction and Irrigation***Rx Only***\"    Product Usage:  Cutting and shaping bone including bones of the spine and cranium.",
      "product_quantity": "10 units",
      "reason_for_recall": "The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.",
      "recall_initiation_date": "20120109",
      "center_classification_date": "20121017",
      "termination_date": "20140916",
      "report_date": "20121024",
      "code_info": "Serial Numbers: E3230327501, E32305327502, E32305327503, E32305327504, E32305327505, E32305327601, E32305327602, E32305327603, E32305327604, and E32305327605"
    }
  ]
}