{
  "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": "Terminated",
      "city": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88687",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "N/A",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution to a single US distributor in Michigan",
      "recall_number": "Z-0147-2022",
      "product_description": "Kit: Central Line Dres Change 20/Cs",
      "product_quantity": "42 cases",
      "reason_for_recall": "The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.",
      "recall_initiation_date": "20210908",
      "center_classification_date": "20211019",
      "termination_date": "20231013",
      "report_date": "20211027",
      "code_info": "Product Code: 59815B, Batch 0000285665; Kit expiration date 03/31/2024    UDI: 20809160170523"
    }
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}