{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tel Aviv-Yafo",
      "state": "",
      "country": "Israel",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88401",
      "recalling_firm": "SIGHT DIAGNOSTICS LTD",
      "address_1": "23, Derekh Menakhem Begin",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of Alabama, Florida,  Massachusetts, Minnesota, Missouri, New York, Ohio, Texas, Virginia, Washington and the countries of AUSTRALIA, CHILE, UNITED KINGDOM, GEORGIA, ISRAEL, Mexico,  NETHERLANDS, Portugal, Russia, Singapore, Thailand.",
      "recall_number": "Z-2517-2021",
      "product_description": "Sight OLO-E1/U1 Software and Operators Manual  Software v2.56.1  Catalog #: 1 OLO-U1    Catalog #: 2 OLO-E1  revision 1.9, revision 1.10",
      "product_quantity": "114 units",
      "reason_for_recall": "Discrepancy in labeling between the adult CBC reference ranges presented in the OLO Operator's Manual and the OLO software",
      "recall_initiation_date": "20210317",
      "center_classification_date": "20210922",
      "termination_date": "20220608",
      "report_date": "20210929",
      "code_info": "Software v2.56.1 Catalog #: 1 OLO-U1   Catalog #: 2 OLO-E1 revision 1.9, revision 1.10",
      "more_code_info": ""
    }
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}