{
  "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": "Crumlin Colorado Antrim",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86238",
      "recalling_firm": "RANDOX LABORATORIES, LTD.",
      "address_1": "34 Diamond Rd",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to  states of: VA, UT, WV and country of : Canada",
      "recall_number": "Z-2966-2020",
      "product_description": "AM1054 Randox Ammonia (NH3), Enzymatic UV Method    For the quantitative in vitro determination of Ammonia in plasma",
      "product_quantity": "143 kits in total",
      "reason_for_recall": "Randox Ammonia reagents are being recalled from the field due to a positive bias of up to 140¿mol/l being observed on patient samples.",
      "recall_initiation_date": "20200730",
      "center_classification_date": "20200914",
      "termination_date": "20210203",
      "report_date": "20200923",
      "code_info": "Catalogue Number: AM1054  GTIN: 05055273200263  Lot #: 512103  batch 512103"
    }
  ]
}