{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Kearneysville",
      "state": "WV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91745",
      "recalling_firm": "Randox Laboratories",
      "address_1": "515 Industrial Blvd",
      "address_2": "N/A",
      "postal_code": "25430-2778",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "PA, OH, WV",
      "recall_number": "Z-1286-2023",
      "product_description": "CRP Immunoturbidimetric reagent. Intended for the quantitative in vitro determination of CRP concentration in serum  Catalogue number: CP3826",
      "product_quantity": "2 kits",
      "reason_for_recall": "The Antibody (R2 reagent) is showing a positive bias compared to previous batches on patient samples. Quality Controls do not show the same bias and will be within range",
      "recall_initiation_date": "20230201",
      "center_classification_date": "20230324",
      "report_date": "20230405",
      "code_info": "GTIN: 05055273201765 Batch: 588434"
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}