{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Zapopan",
      "state": "",
      "country": "Mexico",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98959",
      "recalling_firm": "Oculus Technologies of Mexico, S.A. de C.V.",
      "address_1": "Calle Industria Vidriera 81",
      "address_2": "Industrial Zapopan Norte",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.",
      "recall_number": "Z-2275-2026",
      "product_description": "PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050",
      "product_quantity": "5904 units",
      "reason_for_recall": "The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.",
      "recall_initiation_date": "20260427",
      "center_classification_date": "20260601",
      "report_date": "20260610",
      "code_info": "UDI:00860009268616 Lot: 25G263",
      "more_code_info": ""
    }
  ]
}