{
  "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": "86897",
      "product_res_number": "Z-0615-2010",
      "event_date_initiated": "2009-11-21",
      "event_date_posted": "2010-01-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-10-25",
      "res_event_number": "53941",
      "product_code": "GKG",
      "product_description": "Haematokrit 20 Centrifuge with 2050 Rotor \nTYP #2014-01 and TYP#201424-01.\n\nUsed for the purpose of determining the hematocrit count of a patient sample by way of applying centrifugal force in a manner that separates red blood cells and allows the proportion of red cell mass to plasma to be measured.",
      "code_info": "Units with plastic motor housing.  TYP #2014-01 and TYP#201424-01.",
      "firm_fei_number": "3004578971",
      "recalling_firm": "Hettich Instruments Management I",
      "address_1": "100 Cummings Ctr Ste 130g 100 Cummings Ctr",
      "address_2": "Ste 130g",
      "city": "Beverly",
      "state": "MA",
      "postal_code": "01915-6127",
      "reason_for_recall": "Centrifuge Rotor Failure: may crack, break, and explode outside the centrifuge.",
      "root_cause_description": "Device Design",
      "action": "Hettich Instruments notified Distributors by email on 11/21/09, to the Request For Urgent Action notifications, dated 11/23/2009.  There is a description of how to identify a recalled rotor as well as a description of the replacement metal rotor that is to be used in place of the list of centrifuges affected by this recall.  Customers are to cease using the setup described and contact their distributor or the firm.  The firm will replace the plastic housing with a metal housing.  Questions should be directed to 978-232-3957.",
      "product_quantity": "46 units total",
      "distribution_pattern": "Worldwide Distribution -- USA, including states of CT and IN, and country of Canada.",
      "openfda": {
        "k_number": [
          "K913128",
          "K821803",
          "K925863",
          "K920207",
          "K930415",
          "K955795",
          "K920759",
          "K813033",
          "K890849",
          "K822445",
          "K961803"
        ],
        "registration_number": [
          "3005990076",
          "1067123",
          "3006697110",
          "3006897996",
          "3003799895",
          "1616487",
          "1061932",
          "3014150341",
          "3043009938",
          "3012942167",
          "3008717264",
          "2249760",
          "3012302888",
          "2050012",
          "3009155756",
          "3011816315",
          "2244900",
          "3017065670"
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          "3006697110",
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          "3043009938",
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          "3012302888",
          "3000251573",
          "2050012",
          "3009155756",
          "3011816315",
          "2244900",
          "3000200590",
          "3017065670"
        ],
        "device_name": "Centrifuge, Hematocrit",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.6400",
        "device_class": "2"
      }
    }
  ]
}