{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cambridge",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88294",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of CA, IL, KY, NY, OH, TX, UT, VA.",
      "recall_number": "Z-2323-2021",
      "product_description": "Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte specific reagents (ASR's)",
      "product_quantity": "23 units",
      "reason_for_recall": "May show unexpected locus specific signals in addition to those at 19p13.3. Users may observe faint additional locus specific signals at 9q34",
      "recall_initiation_date": "20210527",
      "center_classification_date": "20210818",
      "termination_date": "20220509",
      "report_date": "20210825",
      "code_info": "Lots 073004 and 072518 (Probe lot 200918-006)."
    }
  ]
}