{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Huntingdon",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82867",
      "recalling_firm": "Cambridge Sensors Limited",
      "address_1": "Units 9 & 10",
      "address_2": "Cardinal Park",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Illinois",
      "recall_number": "Z-2357-2019",
      "product_description": "Microdot Xtra blood glucose test strips",
      "product_quantity": "17,784 (USA)",
      "reason_for_recall": "The firm reported that a faulty cutting/punching machine did not meet specifications after being fitted with new blades and did not correctly \"notch\" BG test strips intended for use in the US. The impacted strips did not fit into the inlet port of the BG meter, therefore resulting in a delay in BG testing and results.",
      "recall_initiation_date": "20180726",
      "center_classification_date": "20190822",
      "report_date": "20190828",
      "code_info": "LOT NUMBERS  7091101, 7091201, 7091801, 7091902, 7100402, 7100403, 7101002, 7101602, 7101702, 7102403, 7103002, 7110602, 7110703, and 7112702."
    }
  ]
}