{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "29837",
      "product_res_number": "Z-0082-04",
      "event_date_initiated": "2003-09-16",
      "event_date_posted": "2003-11-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-04-05",
      "res_event_number": "27415",
      "product_code": "KZH",
      "k_numbers": [
        "K900263"
      ],
      "product_description": "Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm",
      "code_info": "Catalog number AK-25703, Lot number RF3066892",
      "firm_fei_number": "3015859709",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "city": "Reading",
      "state": "PA",
      "postal_code": "19605",
      "additional_info_contact": "Thomas D. Nickel\n610-478-3137",
      "reason_for_recall": "wrong product in box",
      "root_cause_description": "Other",
      "action": "The recalling firm issued a recall letter to their direct customers dated 9/16/03. The recall letter explained the reason for recall and to return the product.",
      "product_quantity": "4480 units",
      "distribution_pattern": "The products were shipped to distributors in AL, AZ, CA, CO, FL, HI, IL, IN, KS, MD, MI, MN, MO, NC, NM, NY, OH, PA,  TN, TX, VA, and WI. The products were shipped to government accounts in AZ, AK, DC, IN, SC, and VA.  The products were shipped to hospitals nationwide.",
      "openfda": {
        "k_number": [
          "K124026",
          "K163400",
          "K073476",
          "K945660",
          "K010377",
          "K872233",
          "K860284",
          "K243232",
          "K051667",
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          "K082587",
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          "K013362",
          "K981266",
          "K951384",
          "K992300",
          "K060141",
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          "K974678",
          "K111467",
          "K141384",
          "K953735",
          "K832847",
          "K032425",
          "K033696",
          "K993385",
          "K160860",
          "K961309",
          "K032848",
          "K834440",
          "K790104",
          "K042557",
          "K945473",
          "K050434",
          "K901803",
          "K060389",
          "K883164",
          "K063146",
          "K974171",
          "K991680",
          "K954729",
          "K970479",
          "K062339",
          "K000482",
          "K862325",
          "K870474"
        ],
        "registration_number": [
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          "3003348846",
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        ],
        "fei_number": [
          "1000219614",
          "2243252",
          "3003166194",
          "3014585508",
          "3005581234",
          "3003346138",
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          "1219205",
          "3003348846",
          "3003974574",
          "3006003617",
          "3004111573",
          "3003131673"
        ],
        "device_name": "Introducer, Syringe Needle",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6920",
        "device_class": "2"
      }
    }
  ]
}