{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "26214",
      "product_res_number": "Z-0634-03",
      "event_date_initiated": "2003-01-24",
      "event_date_posted": "2003-03-12",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-04-28",
      "res_event_number": "25652",
      "product_code": "HMY",
      "k_numbers": [
        "K022637"
      ],
      "product_description": "BD K-3000 Microkeratome Blade\nREF 378607",
      "code_info": "Manufacturing Lot Numbers:  959, 962, 964, 965, and 966",
      "recalling_firm": "BD Opthalmic Systems",
      "address_1": "411 Waverly Oaks Road",
      "city": "Waltham",
      "state": "MA",
      "postal_code": "02452",
      "additional_info_contact": "David Cromwick\n781-906-7916",
      "reason_for_recall": "Microkeratome Blade may cause irregular corneal flap which may delay patients procedure.",
      "root_cause_description": "Other",
      "action": "BD Ophthalmic notified customers by telephone and email on 1/ 24/03. Users are requested to destroy blades and Certify destruction by returning reply form.",
      "product_quantity": "1539 Blades",
      "distribution_pattern": "Nationwide",
      "openfda": {
        "k_number": [
          "K902857",
          "K002191",
          "K022637",
          "K984537",
          "K040297",
          "K022560",
          "K974243",
          "K981741",
          "K992687",
          "K023092",
          "K003594",
          "K781412"
        ],
        "device_name": "Keratome, Battery-Powered",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.4370",
        "device_class": "1",
        "registration_number": [
          "3000264417",
          "3010383847",
          "3016214537",
          "2246552",
          "9615659"
        ],
        "fei_number": [
          "3000264417",
          "3010383847",
          "3003289411",
          "3016214537",
          "2246552"
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      }
    }
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}