{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "186411",
      "product_res_number": "Z-1493-2021",
      "event_date_initiated": "2021-03-19",
      "event_date_created": "2021-04-26",
      "recall_status": "Open, Classified",
      "res_event_number": "87621",
      "product_code": "MVU",
      "product_description": "Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481",
      "code_info": "Lot: RD20/253/16, RD21/043/01, RD21/043/02",
      "firm_fei_number": "3002646096",
      "recalling_firm": "Cytocell Ltd.",
      "address_1": "418 Cambridge Science Park, Milton Road 418 gene technology cambridge science park milton road",
      "city": "Cambridge",
      "country": "United Kingdom",
      "additional_info_contact": "Aysel Parr Heckel\n914-467-5285",
      "reason_for_recall": "Users may observe additional locus specific signals at 9q34. The device pack insert indicates the probe has no known cross-reactivity to 9q34.",
      "root_cause_description": "Under Investigation by firm",
      "action": "On 3/19/2021, Cytocell issued an Urgent Medical Device Recall notice via email notifying customers they may observe additional locus specific signals at 9q34. The device pack insert indicates the probe has no known cross-reactivity to 9q34.",
      "product_quantity": "89 probes",
      "distribution_pattern": "US Nationwide distribution in the states of TX, OH, NY, IL, CT, AL, IA, MO.",
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