{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dublin 15",
      "state": "N/A",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89383",
      "recalling_firm": "Mallinckrodt Pharmaceuticals Ireland Ltd",
      "address_1": "College Business & Technology Park",
      "address_2": "Blanchardstown Road North",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, GA, MA, MI, NC, NJ, NY, OH, TN, TX, VA, WV.",
      "recall_number": "Z-0567-2022",
      "product_description": "THERAKOS CELLEX Photopheresis Procedural Kit, CLXUSA",
      "product_quantity": "3",
      "reason_for_recall": "This recall was initiated to recover a Dunnage Case, which is a case of three (3) CLXUSA kits. This Dunnage Case was shipped on 02-Dec-2021. Dunnage is used during the sterilization process and is not intended for customer use.",
      "recall_initiation_date": "20211210",
      "center_classification_date": "20220207",
      "report_date": "20220216",
      "code_info": "Dunnage case consists of a random unknown lot, which may have been shipped in place of Kit lot K341"
    }
  ]
}