{
  "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": "Cambridge",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92586",
      "recalling_firm": "Cytocell Ltd.",
      "address_1": "418 Cambridge Science Park, Milton Road",
      "address_2": "Oxford Gene Technology",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, OH, & SC.",
      "recall_number": "Z-2209-2023",
      "product_description": "RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.",
      "product_quantity": "60 units",
      "reason_for_recall": "DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.",
      "recall_initiation_date": "20230524",
      "center_classification_date": "20230720",
      "report_date": "20230726",
      "code_info": "Catalog No. LPS508-A; UDI-DI: 05055844900509; Lot No. 076763, 077253, 080125, 080763, 082128, 083041, 083246, 083555.",
      "more_code_info": ""
    }
  ]
}