{
  "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": [
    {
      "status": "Terminated",
      "city": "Watertown",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72326",
      "recalling_firm": "Interactive Motion Technologies, Inc.",
      "address_1": "80 Coolidge Hill Rd",
      "address_2": "N/A",
      "postal_code": "02472-5003",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution to the states of :  Texas and Tennessee., and to the countries of : China, Brazil, Hong Kong, Austria and South Korea.",
      "recall_number": "Z-0199-2016",
      "product_description": "Robotic hand accessory to InMotion Arm, rehabilitation robot.",
      "product_quantity": "8",
      "reason_for_recall": "Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.",
      "recall_initiation_date": "20120505",
      "center_classification_date": "20151102",
      "termination_date": "20170713",
      "report_date": "20151111",
      "code_info": "Serial Numbers: H006, H007, H019, H020, H021, H022, H023, H024. Note: serial numbers may be written with an additional leading 0 (e.g. H0024 instead of H024)"
    }
  ]
}