{
  "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": [
    {
      "country": "United States",
      "city": "Lindon",
      "address_1": "965 W 325 N",
      "reason_for_recall": "TransAmerican Medical Imaging is recalling certain lots of TMI Spectre Wireless Footswitch/Hand switch for GE OEC 9800/9900 and Philips FDS and FDB Cath Labs due to potential safety issue related to the use of this product producing uncommanded X-ray.",
      "address_2": "",
      "product_quantity": "68",
      "code_info": "Serial numbers NS 10324 through NS 10392",
      "center_classification_date": "20140103",
      "distribution_pattern": "US Distribution: including states of: WA and UT.",
      "state": "UT",
      "product_description": "Spectre Wireless Footswitch/Handswitch system Model 98/99, Model FDS, Model FDB.    The Spectre Wireless Encrypted Footswitch/Hand Switch System is a prescription use system and intended only for use with the system indicated in the model number",
      "report_date": "20140115",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Trans American Medical, Inc.",
      "recall_number": "Z-0532-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66064",
      "termination_date": "20151229",
      "more_code_info": "",
      "recall_initiation_date": "20130822",
      "postal_code": "84042",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}