{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Irving",
      "state": "TX",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91303",
      "recalling_firm": "Abbott Laboratories",
      "address_1": "1915 Hurd Dr",
      "address_2": "N/A",
      "postal_code": "75038",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV",
      "recall_number": "Z-0958-2023",
      "product_description": "Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels",
      "product_quantity": "70 cases",
      "reason_for_recall": "Reaction vessels may contain a potential contaminant that could affect their optical performance.",
      "recall_initiation_date": "20221124",
      "center_classification_date": "20230117",
      "report_date": "20230125",
      "code_info": "UDI-DI/Lots: 00380740129026/000586790 and 000586879"
    }
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}