{
  "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": [
    {
      "country": "United States",
      "city": "Palm Beach Gardens",
      "address_1": "4500 Riverside Drive",
      "reason_for_recall": "Anspach was contacted by a hospital to inform Anspach that a Blackmax motor had been used in a case where the patient was diagnosed with Creutzfeldt-Jacob Disease (CJD).",
      "address_2": "",
      "product_quantity": "4 ( BLACKMAX-N) and 1 (Foot Control)",
      "code_info": "Serial # 1934, 3135, 50229989-3, and 31496704 (BLACKMAX-N)  Serial # 80017906 (Foot Control)",
      "center_classification_date": "20140106",
      "distribution_pattern": "US Distribution: Maryland only.",
      "state": "FL",
      "product_description": "Anspach BLACKMAX-N (Pneumatic motor) and Autolube III (Foot Control).    Cutting and shaping bone.",
      "report_date": "20140115",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "The Anspach Effort, Inc.",
      "recall_number": "Z-0631-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "67131",
      "termination_date": "20160418",
      "more_code_info": "",
      "recall_initiation_date": "20120611",
      "postal_code": "33410-4235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}