{
  "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": "Ongoing",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88852",
      "recalling_firm": "Therakos, Inc.",
      "address_1": "10 N High St Ste 300",
      "address_2": "N/A",
      "postal_code": "19380-3014",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "IL",
      "recall_number": "Z-0212-2022",
      "product_description": "THERAKOS CELLEX Photopheresis Procedural Kit PRODUCT CODE:\tCLXUSA",
      "product_quantity": "Five (5) Cases -3 Kits/Case= 15 Kits",
      "reason_for_recall": "Product was released prior to all testing being completed. If used and a drive tube leak were to occur,  may cause illness or injury.",
      "recall_initiation_date": "20211004",
      "center_classification_date": "20211105",
      "report_date": "20211117",
      "code_info": "LOT # K307 EXPIRATION DATE: 2023-02-01 UDI:  (01)20705030200003(10)K307(17)230201",
      "more_code_info": ""
    }
  ]
}