{
  "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": [
    {
      "country": "United States",
      "city": "Palm Beach Gardens",
      "address_1": "4500 Riverside Dr",
      "reason_for_recall": "Supplied Directions for Use (DFU) did not contain a recommended service interval.",
      "address_2": "",
      "product_quantity": "297",
      "code_info": "All serial numbers shipped to customers prior to 09/27/2016; DFU 18-0062; Part No. B-SILVER.",
      "center_classification_date": "20170504",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan",
      "state": "FL",
      "product_description": "6.1CM ATTACHMENT, BLACK MAX    Product Usage:  Pneumatic system",
      "report_date": "20170510",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "The Anspach Effort, Inc.",
      "recall_number": "Z-1980-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76059",
      "termination_date": "20190726",
      "more_code_info": "",
      "recall_initiation_date": "20161006",
      "postal_code": "33410-4235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}