{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87606",
      "recalling_firm": "Gf Health Products",
      "address_1": "1 Graham Field Way",
      "address_2": "N/A",
      "postal_code": "30360-2808",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide to CA, WI, PA, IL, and TX. Distributed internationally to Mexico and Canada.",
      "recall_number": "Z-1353-2021",
      "product_description": "Drop Arm Versamode\"",
      "product_quantity": "66 units",
      "reason_for_recall": "The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.",
      "recall_initiation_date": "20210324",
      "center_classification_date": "20210405",
      "termination_date": "20230501",
      "report_date": "20210414",
      "code_info": "Model: 6810A; Device Identifier: M36868101; and Lot number: BMW316BS"
    }
  ]
}