{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "North Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98502",
      "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 - US Nationwide and the countries of Argentina, Australia, Bhutan, Bolivia, Canada, Chile, Diego Garcia, Ecuador, Eritrea, Georgia, Ghana, Guam, Guatemala, Haiti, Hong Kong, India, Indonesia, Israel, Italy, Ivory Coast, Japan, Kyrgyzstan, Mexico, Nepal, Peru, Philippines, South Africa, South Korea, Spain, UAE, Uruguay, Vietnam.",
      "recall_number": "Z-1894-2026",
      "product_description": "LeadCare¿ Plus Blood Lead Test Kit;  Catalog Number: 82-0004;  The LeadCare¿ Plus kit is provided with the following materials:   \"\tSensors (4 containers of 24 each; 96 tests)   \"\tTreatment Reagent Tubes (4 packages of 24 each; 96 tests)  \"\tCalibration Button (1 @)  \"\tLead Control Level 1 (1 @ 2 mL)  \"\tLead Control Level 2 (1 @ 2 mL)",
      "product_quantity": "136",
      "reason_for_recall": "Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test Systems. False positive lead results may cause delayed results and additional unnecessary testing.",
      "recall_initiation_date": "20260313",
      "center_classification_date": "20260417",
      "report_date": "20260429",
      "code_info": "Catalog Number: 82-0004; UDI-DI: 00850355006031; ALL lots and ALL sublots;",
      "more_code_info": ""
    }
  ]
}