{
  "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": "2026-09-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "218007",
      "product_res_number": "Z-1219-2026",
      "event_date_initiated": "2025-12-22",
      "event_date_posted": "2026-01-29",
      "recall_status": "Open, Classified",
      "res_event_number": "98245",
      "product_code": "OWL",
      "product_description": "LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit",
      "code_info": "Lot Code: Model No. 2519CP; UDI-DI 00661392048157; Lot# 5G3119; Expiration Date 7/31/26\nGTIN: (01)00661392048157(10)5G3119(17)260731",
      "firm_fei_number": "1420054",
      "recalling_firm": "LSL Healthcare Inc.",
      "address_1": "6200 W Howard St",
      "city": "Niles",
      "state": "IL",
      "postal_code": "60714-3404",
      "additional_info_contact": "Demetrius Bridges\n773-878-1100",
      "reason_for_recall": "BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.",
      "root_cause_description": "Under Investigation by firm",
      "action": "LSL issued issued an URGENT:  Kit Component Recall notice to its sole consignee on 12/22/2025 via email.  The notice explained the issue and requested the following actions:  \n\"1.  Immediately stop using the affected kits in your facility.\n2.  Inspect all inventory locations within your facility and destroy all affected kits according to your facility's disposal process. If destruction is not feasible immediately, the products should be quarantined until proper disposal can occur. If disposal is not possible, please request a Return Merchandise Authorization (RMA) to return these kits as indicated below.\n3.  This recall should be executed at the distributor, hospital, and user levels. Identify all customers within your distribution network who may have purchased the affected products listed in this notification. Provide a copy of the attached customer letter to all of these customers to inform them of the recall on behalf of BD & LSL.\n4.  Complete the attached Response Form and return it to the LSL contact provided on the form if you have any of the affected products in stock. This will help LSL acknowledge your receipt of this notification. Please indicate the quantity of affected products identified in your facility and confirm whether this inventory was destroyed or returned.\n5.  If you require assistance with this process, please contact your LSL representative or reach out to LSL using the contact information provided below.  \nLSL Industries LLS, dba LSL Healthcare\n6200 W. Howard Street\nNile, IL, 60714\n(888) 225-5575 | lslorderinquiries@lslhealthcare.com\"  \nLSL will provide credit for any destroyed products from the specific lot numbers mentioned above to customers who purchased the affected items directly from LSL. This will occur upon receipt of the completed Response Form.",
      "product_quantity": "1400 kits",
      "distribution_pattern": "US Nationwide distribution in the state of Idaho.",
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        "fei_number": [
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        ],
        "device_name": "Peripheral Catheter Insertion Kit",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5200",
        "device_class": "2"
      }
    }
  ]
}