{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90818",
      "recalling_firm": "Leica Microsystems, Inc.",
      "address_1": "10 Parkway North blvd ste 300",
      "address_2": "N/A",
      "postal_code": "60089-6622",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1849-2022",
      "product_description": "Leica Surgical Operating Microscopes, Arveo, Part Number 10448999",
      "product_quantity": "25 devices",
      "reason_for_recall": "During internal testing, Leica Microsystems has become aware of a component change on the photodiodes inside the M530 Optics Carrier which will result in an inaccurate adjustment of the illumination limits by the software of the surgical microscope when \"BrightCare Plus\" with Luxmeter is used.",
      "recall_initiation_date": "20220826",
      "center_classification_date": "20220929",
      "report_date": "20221005",
      "code_info": "Serial Numbers:  210721001, 180721001, 190721001, 121021001, 100821001, 60821001, 90821001, 120821001, 10821001, 80721001, 40821001, 130821001, 290821001, 240821001, 91021001, 180921001, 181121001, 151021001, 190821001, 160921001, 20721001, 50721001, 40921001, 150821001, 160821001"
    }
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}