{
  "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": "41880",
      "product_res_number": "Z-0087-06",
      "event_date_initiated": "2005-08-24",
      "event_date_posted": "2005-10-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-03-24",
      "res_event_number": "33435",
      "product_code": "JJC",
      "product_description": "Y-valve and T-valve, PSD/4 Syringe Drive Module parts.",
      "code_info": "catalog number 7427-01 (Y-valve), catalog number 7990-01 (T-valve), catalog number 51863-01-IL (PSD/4 with valve and syringe), no 510k number.  For 7427-01 (Lot number, date of manufacture):  277702, 4/29/2003; 282550A, 8/11/2003; 282550, 8/13/2003; 286630, 10/1/2003; 287449, 10/20/2003; 287137, 10/20/2003; 287949, 12/18/2003; 301809, 6/30/2004; 305599, 8/19/2005; 309328, 11/5/2004; 313276, 12/17/2004; 314662, 3/7/2005; 317940, 4/6/2005; 319506, 4/11/2005; 321121, 5/6/2005; 324204, 6/23/2005; 325483, 7/20/2005.  For 7990-01:  277703, 4/30/2003; 283119, 9/30/2003 291279, 1/7/2004; 303942, 7/19/2004; 303687, 7/19/2004; 318833, 3/24/2005; 319684, 5/5/2005.",
      "firm_fei_number": "2915796",
      "recalling_firm": "Hamilton Co",
      "address_1": "4970 Energy Way",
      "city": "Reno",
      "state": "NV",
      "postal_code": "89502-4123",
      "reason_for_recall": "The product valve has a high probability of deforming and may result in leakage during use.",
      "root_cause_description": "Other",
      "action": "Recall initiated on 08/24/2005.  The firm issued notification to its consignees via overnight letter, and via e-mail for its distributor (Hamilton Bonaduz).",
      "product_quantity": "271 Y and 78 T valves were distributed.",
      "distribution_pattern": "One distributor and 8 consumers received this product in CA, MA, MI, WI, Japan and Switzerland.",
      "openfda": {
        "k_number": [
          "K881056",
          "K945915",
          "K771336",
          "K901410",
          "K823233",
          "K833157",
          "K781503",
          "K760622",
          "K854345",
          "K833023",
          "K800453",
          "K771662",
          "K761165",
          "K801481",
          "K862561",
          "K852306",
          "K870998",
          "K761086",
          "K813077",
          "K761342",
          "K945584",
          "K770506",
          "K811249",
          "K760749",
          "K810394",
          "K901141",
          "K760211",
          "K943376",
          "K792285",
          "K875105",
          "K800587",
          "K890332"
        ],
        "device_name": "Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.2150",
        "device_class": "1",
        "registration_number": [
          "3016837106",
          "3003741796",
          "",
          "3012275122",
          "8030996",
          "1219029",
          "2432235",
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          "3018771894",
          "3043088937",
          "3027645317",
          "3043138885",
          "3010402964",
          "2016673"
        ],
        "fei_number": [
          "3016837106",
          "3003741796",
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          "3012275122",
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      }
    }
  ]
}