{
  "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": "Ongoing",
      "city": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92483",
      "recalling_firm": "p-Chip Corporation",
      "address_1": "500 W Madison St",
      "address_2": "Suite 1000",
      "postal_code": "60661-4544",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1693-2023",
      "product_description": "p-Chip Wand Reader",
      "product_quantity": "329 units",
      "reason_for_recall": "The laser operation might fall under a higher laser class.",
      "recall_initiation_date": "20210303",
      "center_classification_date": "20230612",
      "report_date": "20230621",
      "code_info": "Model: WA-4000, 4500, -8000, and -8500"
    }
  ]
}