{
  "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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  "results": [
    {
      "status": "Ongoing",
      "city": "Wetzlar",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92847",
      "recalling_firm": "Oculus Optikgeraete GMBH",
      "address_1": "Munchholzhauser Str. 29",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
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      "product_description": "Oculus Pentacam AXL , Ref 70100, CE 0123",
      "product_quantity": "364 units",
      "reason_for_recall": "Their is a potential that  optical devices with insufficient anti-reflective coating  may lead to incorrect axial length measurements.",
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      "code_info": "UDI-DI; (01) 04049584012333"
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