{
  "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": "113401",
      "product_res_number": "Z-0107-2013",
      "event_date_initiated": "2011-01-18",
      "event_date_posted": "2012-10-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-10-22",
      "res_event_number": "63276",
      "product_code": "CBT",
      "product_description": "Pulset Arterial Blood Gas (ABG) sampling kit.\n\nFull Kit, Pulset, 3 cc, w/Crickett 23g x 1\" A Needle, 25U Balanced Heparin, part number: 3373-95.\n\nAn arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.",
      "code_info": "Lot Numbers:  38784, 39142, 39144, 39145, 39211, 39137, 39141, 39322, 39321, 39629, 39628, 39630, 39830, 39831, 39832, 40424, 40625, 40950, 41402, 41415, 42070, 42416, 42517, 42858, 43325, 43196, 43577, 43982, 44146, 44678, 45562, 45671, 45826, 46340, 46470, 46780, 46779, 47081, 47174, 47370,47487, 47597, 47606, 47847, 48484, 48580, 48625, 48811, 48860, 48896, 49036, 49260, 49357, 49473, 49569, 49906.",
      "firm_fei_number": "1000374126",
      "recalling_firm": "Westmed Inc",
      "address_1": "5580 S Nogales Hwy Ste 170 5580 S Nogales Hwy",
      "address_2": "Ste 170",
      "city": "Tucson",
      "state": "AZ",
      "postal_code": "85706-3333",
      "additional_info_contact": "520-294-7987 Ext. 1233",
      "reason_for_recall": "Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.",
      "root_cause_description": "Material/Component Contamination",
      "action": "Westmed sent an \"URGENT: MEDICAL DEVICE RECALL\" letter dated January 18, 2011 to all affected customers.  The letter identified the product, problem, and actions to be taken by the customers.  Customers were also given the TRIAD GROUP:  \"Urgent Drug Recall\" and \"Facts:  Alcohol Recall\" both dated January 3, 2011.  Westmed customers were instructed to remove  the TRIAD alcohol pad from the kit and dispose of the alcohol pad only.  Customers were instructed to complete and return the enclosed response form as soon as possible.  Customers with questions were instructed to contact the firm at (520) 264-7987 x1233.",
      "product_quantity": "1,259,200 units total",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Canada, El Salvador, United Arab Emirates, Holland, Costa Rica and Lebanon.",
      "openfda": {
        "k_number": [
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        "registration_number": [
          "1423537",
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        "fei_number": [
          "3009888344",
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          "3016707060",
          "3002558692",
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          "3005587132",
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        ],
        "device_name": "Arterial Blood Sampling Kit",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.1100",
        "device_class": "1"
      }
    }
  ]
}