{
  "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": "Terminated",
      "city": "Lake Zurich",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87407",
      "recalling_firm": "Fenwal Inc",
      "address_1": "3 Corporate Dr Ste 300",
      "address_2": "N/A",
      "postal_code": "60047-8930",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of GA, TX, TN, MD, CA, KS, MN, MA, NM, NC, LA, CO, KY, NV, PA, UT, MI, NJ, IL, MD, OH, NY, FL.",
      "recall_number": "Z-1345-2021",
      "product_description": "Amicus Exchange Kit Therapeutics - Product Usage: intended for use in the collection of blood components and mononuclear cells.",
      "product_quantity": "24 units",
      "reason_for_recall": "Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking centrifuge packs  during a procedure on the Amicus Separator using therapeutic protocols only. The defect is a  blood leak at the boot, elbow, or in the channel on the separation chamber of the centrifuge pack.",
      "recall_initiation_date": "20210225",
      "center_classification_date": "20210402",
      "termination_date": "20230418",
      "report_date": "20210414",
      "code_info": "Product Code X6R2349; UDI: 04086000101950; Batch Numbers FA20E25150 (Exp. 05/31/2022) and FA20I22142  (Exp. 09/30/2022)"
    }
  ]
}