{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Fremont",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94086",
      "recalling_firm": "Think Surgical, Inc.",
      "address_1": "47201 Lakeview Blvd",
      "address_2": "",
      "postal_code": "94538-6530",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, OH, NV, TX, UT, CA, MO.",
      "recall_number": "Z-1318-2024",
      "product_description": "Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System",
      "product_quantity": "16",
      "reason_for_recall": "There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner diameter of the TMINI array guide holes. As a result, the array guide has the possibility of binding to the array fixation pins during drilling.",
      "recall_initiation_date": "20240212",
      "center_classification_date": "20240320",
      "report_date": "20240327",
      "code_info": "UDI-DI: M9461091010.  Lot Numbers: 2316701, 2232601, 23030, 2228501, 2327802, 22152",
      "more_code_info": ""
    }
  ]
}