{
  "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": "2026-03-18",
    "results": {
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    {
      "status": "Terminated",
      "city": "Maastricht-Airport",
      "state": "",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90733",
      "recalling_firm": "Technomed Europe",
      "address_1": "Amerikalaan 71",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1737-2022",
      "product_description": "Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.",
      "product_quantity": "37/25-electrode boxes",
      "reason_for_recall": "Burns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU.",
      "recall_initiation_date": "20220809",
      "center_classification_date": "20220912",
      "termination_date": "20240411",
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      "code_info": "Lot numbers 044220, exp. 1/1/2023; 045077, exp. 3/1/2023; 045443, exp. 4/1/2023; and 049285, exp. 7/1/2024;  UDI-DI 08718375861530.",
      "more_code_info": ""
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}