{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88104",
      "recalling_firm": "CAREFUSION",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "N/A",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: TN    O.U.S.: None",
      "recall_number": "Z-1995-2021",
      "product_description": "MaxPlusTM bi fuse extension set with 2 clear needleless connectors - Product Usage:  The needleless connector can be used for direct injection, intermittent infusion, continuous infusion, or aspiration.",
      "product_quantity": "100 units",
      "reason_for_recall": "A portion of a validation lot was inadvertently released to the US Market.  The product did not meet the validation testing criteria regarding leakage.",
      "recall_initiation_date": "20210609",
      "center_classification_date": "20210701",
      "termination_date": "20240708",
      "report_date": "20210707",
      "code_info": "Catalog Number:MP9246-C  GTIN: 10885403237157  Lot Number: 20087194"
    }
  ]
}