{
  "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": "Terminated",
      "city": "Torrance",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78595",
      "recalling_firm": "EAI-JR286 INC",
      "address_1": "20100 S Vermont Ave",
      "address_2": "N/A",
      "postal_code": "90502-1361",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide in the USA and Puerto Rico.",
      "recall_number": "D-0100-2018",
      "product_description": "Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun Protection Cream, SPF 50+, Net. Wt. 2.8 oz (80 g) tube in a carton, Distributed by Vertra/EAI-JR286, 20100 S Vermont Ave, Torrance, CA 90502, Made In Australia, UPC 8 94140 00103 0.",
      "product_quantity": "5,355 tubes",
      "reason_for_recall": "CGMP Deviations: products manufactured in a manner that may impact product quality that includes but is not limited to failed viscosity.",
      "recall_initiation_date": "20171128",
      "center_classification_date": "20171130",
      "termination_date": "20190809",
      "report_date": "20171206",
      "code_info": "Lot #: 609124, Exp 03/18    Manufacturing batches were mfg at Delta Laboratories under Batch Number 511103 11/16/2015  Batch Number 609124 09/21/2016"
    }
  ]
}