{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Heverlee",
      "state": "N/A",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92621",
      "recalling_firm": "Materialise N.V.",
      "address_1": "Technologielaan 15",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "International Distribution to countries of: Germany, Netherlands",
      "recall_number": "Z-2213-2023",
      "product_description": "MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR.  Ref: KNM-ZB02-00-01",
      "product_quantity": "2 Guides",
      "reason_for_recall": "The wrong tibia guide was included intended for a different patient case.",
      "recall_initiation_date": "20230426",
      "center_classification_date": "20230720",
      "report_date": "20230726",
      "code_info": "UDI-DI: (01)05420060310027 Lot Number/Case Number:  ZB22UHINEF,  ZB23MANOLA",
      "more_code_info": ""
    }
  ]
}