{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "50158",
      "product_res_number": "Z-0565-2007",
      "event_date_initiated": "2006-12-22",
      "event_date_posted": "2007-03-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-11-28",
      "res_event_number": "37234",
      "product_code": "GIF",
      "k_numbers": [
        "K051215",
        "K061667",
        "K961439"
      ],
      "product_description": "CELL-DYN Diluent/Sheath Reagent, for use with CELL-DYN Ruby, Sapphire and 4000 systems.  List #01H73-01.  Packaged in 20 Liter cubitainers.",
      "code_info": "Lot Number 42063I2, List Number 01H73-01",
      "firm_fei_number": "2919069",
      "recalling_firm": "Abbott Laboratories",
      "address_1": "5440 Patrick Henry Dr",
      "city": "Santa Clara",
      "state": "CA",
      "postal_code": "95054-1113",
      "reason_for_recall": "Results for tests of RBC, MCV, RDW, MPV and PLT  may be falsely elevated or falsely decreased when the Cell Dyn Diluent/Sheath reagent is used with Cell-Dyn 4000, Ruby and Sapphire systems.",
      "root_cause_description": "Other",
      "action": "Recall initated 12/22/2006.  Product letters were sent to consignees, as well as a customer reply form.  The letters were sent with customer reply forms.  Responses will be tracked via the response forms included with letters.",
      "product_quantity": "652 (20 L. each) cubitainers",
      "distribution_pattern": "Nationwide, including California and Nevada.  \nAn Abbott Laboratories facility in Hong Kong.",
      "openfda": {
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        "device_name": "Diluent, Blood Cell",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.8200",
        "device_class": "1",
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