{
  "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": "Brooklyn Park",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87915",
      "recalling_firm": "Medtronic Perfusion Systems",
      "address_1": "7611 Northland Dr N",
      "address_2": "",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX.  There was no foreign/government/military distribution.",
      "recall_number": "Z-1882-2021",
      "product_description": "Medtronic CB10W64R1, Custom Pack CB10W64R1 CH Access 3/8, Custom Perfusion System, Sterile, Rx.",
      "product_quantity": "12 tubing packs",
      "reason_for_recall": "Specific lots may have been manufactured with insufficient or incomplete welds.",
      "recall_initiation_date": "20210429",
      "center_classification_date": "20210616",
      "termination_date": "20230320",
      "report_date": "20210623",
      "code_info": "GTIN 00763000341015, Lot numbers 221102372, Use By 2022-09-21; and 221672013, Use By 2022-11-02",
      "more_code_info": ""
    }
  ]
}