{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "141071",
      "product_res_number": "Z-0199-2016",
      "event_date_initiated": "2012-05-05",
      "event_date_posted": "2015-11-02",
      "recall_status": "Terminated",
      "event_date_terminated": "2017-07-13",
      "res_event_number": "72326",
      "product_code": "IKK",
      "product_description": "Robotic hand accessory to InMotion Arm, rehabilitation robot.",
      "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)",
      "firm_fei_number": "3002758968",
      "recalling_firm": "Interactive Motion Technologies, Inc.",
      "address_1": "80 Coolidge Hill Rd",
      "city": "Watertown",
      "state": "MA",
      "postal_code": "02472-5003",
      "reason_for_recall": "Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.",
      "root_cause_description": "Component design/selection",
      "action": "Interactive Motion Technology ( IMT) sent an Important Patient Safety Information letter dated March 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.\n\nSummary of Actions to be taken For Hand Robot Cover B, firm recommends continued vigilance for both Adult and Pediatric Patients while in contact with this group of devices. For Hand Robot Covers A or C, at clinician discretion based on expected patient population, firm recommends continued use when appropriate of the IMT supplied Hypertonia Spring Assembly, or if not appropriate, insertion of the IMT Zero Force Spring Assembly. IMT will make this kit available for each Hand Robot upon request, or insert the Assembly when the Hand Robot is shipped to IMT using the special shipping container. \n\nIf you have any questions, please contact your local IMT Representative or IMT Technical Services at support@interactive-motion.com.",
      "product_quantity": "8",
      "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.",
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        "device_name": "System, Isokinetic Testing And Evaluation",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.1925",
        "device_class": "2"
      }
    }
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}