{
  "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": "2026-10-21",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "North Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99776",
      "recalling_firm": "Magellan Diagnostics, Inc.",
      "address_1": "101 Billerica Ave Bldg 4",
      "address_2": "",
      "postal_code": "01862-1271",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of CA, IN, PA, TX, NE, IL, MA, MO, KY.",
      "recall_number": "Z-0162-2027",
      "product_description": "LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.",
      "product_quantity": "321 units",
      "reason_for_recall": "In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct expiration date is July 13, 2026.  If used the system will display an error message and prevent the operator from running the test. Resulting in delayed results.",
      "recall_initiation_date": "20260904",
      "center_classification_date": "20261015",
      "report_date": "20261021",
      "code_info": "Model/Catalog Number: 70-6762. UD-DI: 00850355006000. Lot Number. 2530M-01.",
      "more_code_info": ""
    }
  ]
}