{
  "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": "North Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87992",
      "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. US nationwide including Puerto Rico; Canada, Vietnam, India, Italy, Peru, New Zealand, Australia, Hong Kong, and Philippines.",
      "recall_number": "Z-1953-2021",
      "product_description": "LeadCare Plus Blood Lead Test Kit  Catalog Number  \t82-0004",
      "product_quantity": "320 kits (96 tests/kit=30,720 tests)",
      "reason_for_recall": "Magellan has received reports that control tests of either the Low-Control and/or the High-Control generated a low result. The issue may cause the underestimation of blood lead levels in patient samples.",
      "recall_initiation_date": "20210507",
      "center_classification_date": "20210701",
      "termination_date": "20231024",
      "report_date": "20210707",
      "code_info": "Lot Numbers/Expiration Date: 2011MU - 25MAR22.  1st expansion 6/21/2021:  2104MU - 25AUG22; 2108MU - 31MAR22."
    }
  ]
}