{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95028",
      "recalling_firm": "EVIDENT SCIENTIFIC INC",
      "address_1": "48 Woerd Ave",
      "address_2": "N/A",
      "postal_code": "02453-3826",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US",
      "recall_number": "Z-2416-2024",
      "product_description": "SlideView VS200 slide viewer,",
      "product_quantity": "N/A",
      "reason_for_recall": "A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly  positioned cable that made contact with the housing/frame and caused a short  circuit and destroyed the fuse in the laser. This caused the shutter to remain in its  most recent state; either in an open or closed position. Once the fuse was destroyed  the shutter could not be operated.",
      "recall_initiation_date": "20240722",
      "center_classification_date": "20240726",
      "report_date": "20240807",
      "code_info": "65159 67105 67104 69153 67106 69154"
    }
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}