{
  "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": "64247",
      "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 - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden.    .",
      "recall_number": "Z-1900-2014",
      "product_description": "ANSPACH***REF 98-0044***Custom Device Speed Reducer with Bumper***Rx Only***    This device is intended to be used with Anspach Systems",
      "product_quantity": "2",
      "reason_for_recall": "The Anspach Effort, Inc.  in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements.",
      "recall_initiation_date": "20121128",
      "center_classification_date": "20140625",
      "termination_date": "20140807",
      "report_date": "20140702",
      "code_info": "Part Number: 98-0044; Serial Number: E16200088601."
    }
  ]
}