{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lugano",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79645",
      "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": "Distributors in 2 states: NY and IL.",
      "recall_number": "Z-1798-2018",
      "product_description": "FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System",
      "product_quantity": "18",
      "reason_for_recall": "Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to patients.",
      "recall_initiation_date": "20180213",
      "center_classification_date": "20180510",
      "termination_date": "20190403",
      "report_date": "20180516",
      "code_info": "Serial Numbers:   Accelerator a3600 -   ACP.150  ACP.185  ACP.186  ACP.192  ACP.202  ACP.214    FlexLab - FLX.0165  FLX.0127  FLX.0128  FLX.0133  FLX.0157  FLX.0160  FLX.0181    Aptio Automation -  AP2.0054  AP2.0056  AP2.0060  AP2.0078  AP2.0095    Part Numbers of impacted sample tube carriers: 721501001 for 43 mm carriers, and 0A00006957 for 40 mm carriers"
    }
  ]
}