{
  "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": "N Charleston",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65062",
      "recalling_firm": "Berchtold Corp.",
      "address_1": "1950 Hanahan Rd",
      "address_2": "N/A",
      "postal_code": "29406-4878",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-1488-2013",
      "product_description": "Hand Controls for Operon D750, D752, D760, D820 and D850    The hand controls are used to operate OPERON surgical tables",
      "product_quantity": "3763",
      "reason_for_recall": "The firm received complaints for unintended movements.",
      "recall_initiation_date": "20130312",
      "center_classification_date": "20130606",
      "termination_date": "20170508",
      "report_date": "20130612",
      "code_info": "The hand controls are neither serialized nor lot coded."
    }
  ]
}