{
  "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": "43266",
      "product_res_number": "Z-0430-06",
      "event_date_initiated": "2005-12-01",
      "event_date_posted": "2006-01-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-04-06",
      "res_event_number": "34202",
      "product_code": "JQX",
      "product_description": "BD PhoenixSpec Calibrator Kit, consisting of 3  tubes identified as 0.25, 1.0 and 4.0 McFarland unit calibrators, and labeled in part ***Becton, Dickinson and Company, 7 Loveton Circle, Sparks, MD 21152 USA***",
      "code_info": "Lot 5075281 Exp 2/14/06*** Lot 5115146 Exp 2/14/06",
      "firm_fei_number": "1119779",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Cir",
      "city": "Sparks",
      "state": "MD",
      "postal_code": "21152-9212",
      "additional_info_contact": "BD Technical Services Dept\n800-638-8663 Ext. 2",
      "reason_for_recall": "A calibrator for an in vitro diagnostic kit is not standarized correctly and may cause a calibration error when measuring microbiological cultures for turbidity.",
      "root_cause_description": "Other",
      "action": "The recalling firm notified consignees by phone, fax and e-mail on 12/01/05. The notification advised that  nephelometers displaying 'CAL' error messages on the LED should not be used until calibrated with a different kit lot. Consignees were requested to discard referenced lots for replacement. A response form was included in the notification.",
      "product_quantity": "145 kits",
      "distribution_pattern": "Product was sold to direct accounts nationwide and international affiliated distributors in Japan, Belize, Taiwan, Canada, Korea, Australia, and the Philippines.",
      "openfda": {
        "k_number": [
          "K885263",
          "K962294",
          "K801362",
          "K771446",
          "K851253",
          "K851234",
          "K781554",
          "K772361",
          "K781644",
          "K780251",
          "K792045",
          "K801089",
          "K790103",
          "K922273"
        ],
        "registration_number": [
          "2050012",
          "1111096",
          "3009238284",
          "3008517993",
          "3008862790",
          "3038188172",
          "1530126",
          "1119779",
          "3027977508",
          "3006198300",
          "3006786907",
          "1924669",
          "8021914"
        ],
        "fei_number": [
          "2050012",
          "1111096",
          "3009238284",
          "3008517993",
          "3008862790",
          "3038188172",
          "1119779",
          "3027977508",
          "1000515493",
          "3006198300",
          "3002806332",
          "3006786907",
          "1924669"
        ],
        "device_name": "Nephelometer, For Clinical Use",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.2700",
        "device_class": "1"
      }
    }
  ]
}