{
  "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": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92143",
      "recalling_firm": "Binx Health, Inc.",
      "address_1": "245 1st St Ste 18",
      "address_2": "Riverview II",
      "postal_code": "02142-1292",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "In the US state of PA",
      "recall_number": "Z-1626-2023",
      "product_description": "binx io CT/NG Assay- Single-use Cartridge for the qualitative detection of Chlamydia trachomatis and Neisseria gonorrhoeae    Ref: 1.002.101",
      "product_quantity": "50 single-use cartridges",
      "reason_for_recall": "May not meet the declared performance characteristics for the detection of Chlamydia trachomatis (CT) within the labeled expiry period, potential to produce either false negative CT or positive CT results",
      "recall_initiation_date": "20230329",
      "center_classification_date": "20230523",
      "report_date": "20230531",
      "code_info": "UDI: 5060441760050 Lot Number: 00210869309 Exp Date: March 31, 2023"
    }
  ]
}