{
  "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,
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  },
  "results": [
    {
      "cfres_id": "54235",
      "product_res_number": "Z-0066-2008",
      "event_date_initiated": "2007-08-09",
      "event_date_posted": "2007-10-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-02-29",
      "res_event_number": "38739",
      "product_code": "HMY",
      "k_numbers": [
        "K023092"
      ],
      "product_description": "BD  Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD)",
      "code_info": "All serial numbers",
      "firm_fei_number": "1211998",
      "recalling_firm": "Becton Dickinson and Company",
      "address_1": "411 Waverley Oaks Rd Ste 2229 411 Waverley Oaks Rd",
      "address_2": "Ste 2229",
      "city": "Waltham",
      "state": "MA",
      "postal_code": "02452-8448",
      "additional_info_contact": "David Cromwick \n781-906-7916",
      "reason_for_recall": "Microkeratome blade may stop oscillating and transverse the eye causing injury to the cornea",
      "root_cause_description": "Component design/selection",
      "action": "BD Medical notified customers by Advisory Letter dated 8/09/07, advising users to return heads and  bearing cartridges for replacement of the o-ring.",
      "product_quantity": "256 units",
      "distribution_pattern": "Worldwide",
      "openfda": {
        "k_number": [
          "K981741",
          "K022560",
          "K023092",
          "K984537",
          "K781412",
          "K003594",
          "K902857",
          "K992687",
          "K022637",
          "K002191",
          "K974243",
          "K040297"
        ],
        "device_name": "Keratome, Battery-Powered",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.4370",
        "device_class": "1",
        "registration_number": [
          "3016214537",
          "3010383847",
          "9615659",
          "3000264417",
          "2246552"
        ],
        "fei_number": [
          "3003289411",
          "3016214537",
          "3010383847",
          "3000264417",
          "2246552"
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      }
    }
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}