{
  "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": "Lugano",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97887",
      "recalling_firm": "Inpeco S.A.",
      "address_1": "Via San Gottardo 10",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Domestic: MI. OUS International: Australia, Finland, France, Germany, Italy, Portugal, Spain, and UK.",
      "recall_number": "Z-0596-2026",
      "product_description": "FlexLab (FLX);  Version: FLX-217-40;",
      "product_quantity": "14 units (1 US, 13 OUS)",
      "reason_for_recall": "The Aliquoter Module (mALX) may  generate secondary sample tubes without labels or with mismatched labels which may result in  delayed results or erroneous results, this error occurs if the operators open the printer head of  mALX to perform error recoveries or maintenance procedures and do not empty the printer  tubes buffer to remove all the secondary sample tubes",
      "recall_initiation_date": "20251030",
      "center_classification_date": "20251125",
      "report_date": "20251203",
      "code_info": "UDI-DI: 07640172344002; Serial number: FXX.0004, FXX.0006, FXX.0009, FXX.0022, FXX.0023, FXX.0024, FXX.0027, FXX.0028, FXX.0034, FXX.0036, FXX.0041, FXX.0042, FXX.0043, FXX.0046;",
      "more_code_info": ""
    }
  ]
}