{
  "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": "Ongoing",
      "city": "Dieren",
      "state": "",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83910",
      "recalling_firm": "Vital Scientific N.V.",
      "address_1": "24, Kanaalweg",
      "address_2": "Postbus 100",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "NY",
      "recall_number": "Z-0547-2020",
      "product_description": "V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180",
      "product_quantity": "732 instruments",
      "reason_for_recall": "During in-house testing it was  determined that their is a possibility that during a sample run, the instrument may aspirate a sample from the wrong sample container resulting  in a sample result and patient ID mismatch. If not detected, this may lead to an incorrect patient report.",
      "recall_initiation_date": "20181115",
      "center_classification_date": "20191122",
      "report_date": "20191204",
      "code_info": "(OUS) V-Twin¿ 6002-800 serial numbers from 3-3021 till 18-3345;  (US) V-Twin¿6002-850 serial numbers from 3-3006 till 9-4037",
      "more_code_info": ""
    }
  ]
}