{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Jamestown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89088",
      "recalling_firm": "Clark Laboratories, Inc.",
      "address_1": "2823 Girts Rd",
      "address_2": "",
      "postal_code": "14701-9666",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "OH, UT",
      "recall_number": "Z-0382-2022",
      "product_description": "Bartels Legionella Urinary Antigen- an adjunct to culture for the presumptive diagnosis of past or current Legionnaire's Disease by qualitative detection of Legionella Pneumophila seragroup 1 antigen in human urine.  Product Code: B1029-440",
      "product_quantity": "53 units",
      "reason_for_recall": "Contamination of the conjugate may cause a pipetting issue which then could lead to an invalid assay",
      "recall_initiation_date": "20211011",
      "center_classification_date": "20211215",
      "termination_date": "20230309",
      "report_date": "20211222",
      "code_info": "Lot # 056  Expiration Date: 2022-11-28 UDI: 05391516744065",
      "more_code_info": ""
    }
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}