{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "West Henrietta",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91607",
      "recalling_firm": "CooperVision, Inc.",
      "address_1": "180 Thruway Park Dr",
      "address_2": "N/A",
      "postal_code": "14586-9798",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, OH, NC, PA.",
      "recall_number": "Z-1198-2023",
      "product_description": "Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (extended wear)",
      "product_quantity": "4 units",
      "reason_for_recall": "Manufactured with misaligned axis resulting in  lenses with the incorrect power, users may experience poor visual acuity",
      "recall_initiation_date": "20230126",
      "center_classification_date": "20230301",
      "report_date": "20230308",
      "code_info": "UDI: N/A Lot Numbers: R24395839, R24406094, R24409954",
      "more_code_info": ""
    }
  ]
}