{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bedford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79165",
      "recalling_firm": "Instrumentation Laboratory Co.",
      "address_1": "180 Hartwell Rd",
      "address_2": "N/A",
      "postal_code": "01730-2443",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "recall_number": "Z-0895-2018",
      "product_description": "Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400",
      "product_quantity": "14,894 kits",
      "reason_for_recall": "Instrumentation Laboratory Co. received customer reports of performance issues with some vials of Lot Nos. N1166235 and N0177760, including increased imprecision, out of range quality controls and prolonged sample results.",
      "recall_initiation_date": "20170802",
      "center_classification_date": "20180303",
      "termination_date": "20190329",
      "report_date": "20180314",
      "code_info": "Lots: N1166235, N0177760, N0278358, N0478057, N0479504 & N0278177."
    }
  ]
}