{
  "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": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87722",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed US nationwide to OH, OR, FL and CA.",
      "recall_number": "Z-1554-2021",
      "product_description": "Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420",
      "product_quantity": "30 cases (20 kits per case)",
      "reason_for_recall": "Medical convenience kits are being recalled due to a potential breach in the package integrity  of a component, the BD ChloraPrep 3mL applicator.",
      "recall_initiation_date": "20210409",
      "center_classification_date": "20210512",
      "termination_date": "20231003",
      "report_date": "20210519",
      "code_info": "Kit Number: 79420; UDI (GTIN): 20809160247775; Lot Number: 0000276767 (Expiration Date: 01/31/2022), 0000278361 (Expiration Date: 05/31/2022), and 0000281458 (Expiration Date: 08/31/2022)",
      "more_code_info": ""
    }
  ]
}