{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "North Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79279",
      "recalling_firm": "Magellan Diagnostics, Inc.",
      "address_1": "101 Billerica Ave Bldg 4",
      "address_2": "N/A",
      "postal_code": "01862-1271",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution",
      "recall_number": "Z-1295-2018",
      "product_description": "LeadCare II Blood Lead Analyzer  Part Numbers: 70-6760, 70-6529-R, 70-6760-P,  70-6760-R.    Intended for in vitro (external) use only.",
      "product_quantity": "6,143",
      "reason_for_recall": "The incorrect placement of AA batteries into certain LeadCare II Blood Lead Analyzer may cause the batteries to overheat, and the chance that a user could burn their fingers if the batteries are removed while hot.",
      "recall_initiation_date": "20180109",
      "center_classification_date": "20180403",
      "termination_date": "20201211",
      "report_date": "20180411",
      "code_info": "Part Numbers: 70-6760, 70-6529-R, 70-6760-P, and   70-6760-R.  All LeadCare II and LeadCare Plus Blood Lead Analyzers with battery boards versions B and O."
    }
  ]
}