{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "30396",
      "product_res_number": "Z-0264-04",
      "event_date_initiated": "2003-11-10",
      "event_date_posted": "2003-12-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-04-05",
      "res_event_number": "27714",
      "product_code": "HJM",
      "k_numbers": [
        "K940393"
      ],
      "product_description": "CX9625 Light Pipe (25 Gauge). The product is sold in packs containing six pipes.",
      "code_info": "Lot numbers: 207089, 209102, 02121321, 02171838, 02192048, 02212272, 02222332, 02242552, 02262741, 02272856, 02293066, 02313269, 02323381, 02333458, 02363752, 02383927, 02404141, 02414225, 02424507, 02434421, 02434520, 02444529, 02454627, 02454672, 02464725, 02474823, 02484921, 02505121, 03020326, 03040522, 03040669, 03060728, 03060803, 03060865, 03080924, 03101124, 03111222, 03131428, 03151624, 03171820, 03171998, 03192023, 03212226, 03212370, 03232422, 03242537, 03252628, 03262726, 03303276, and 03303313.",
      "firm_fei_number": "1317628",
      "recalling_firm": "Bausch & Lomb Inc",
      "address_1": "1400 Goodman St N",
      "city": "Rochester",
      "state": "NY",
      "postal_code": "14609-3547",
      "additional_info_contact": "Glenn A. Davies\n585-338-8215",
      "reason_for_recall": "The CX9625 Light Pipe connector may overheat; this condition could result in the plastic connector that plugs into the Millennium Microsurgical System to malfunction.",
      "root_cause_description": "Other",
      "action": "The recalling firm issued a recall notification dated 11/13/03 to their direct accounts. The recall notification explains the problem and return the product.",
      "product_quantity": "2500 packs",
      "distribution_pattern": "The product was shipped to hospitals/medical facilities and physicians in AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NJ, NH, NY, NC, OH, PA, TN, TX, UT, VA, WA, WI, and WV. Nationwide.  The product was also shipped to Puerto Rico, Argentina, Australia, Brazil, Canada, China, Hong, Kong, India, Japan, Korea, Malaysia, Mexico, New Zealand, The Netherlands, Philippines, Singapore, Spain, Taiwan, and Thailand.",
      "openfda": {
        "k_number": [
          "K811108",
          "K940393",
          "K931072",
          "K893170",
          "K913273",
          "K934269",
          "K933445",
          "K812949",
          "K950529",
          "K945877",
          "K972506",
          "K894513"
        ],
        "device_name": "Transilluminator, Ac-Powered",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.1945",
        "device_class": "2",
        "registration_number": [
          "3013002167",
          "2918630",
          "2521877",
          "1000391004",
          "2183446",
          "1315756",
          "3016798774",
          "3009106214",
          "2025917",
          "2246552",
          "1000379039",
          "1423662"
        ],
        "fei_number": [
          "2521877",
          "2918630",
          "2183446",
          "1000391004",
          "1315756",
          "3016798774",
          "3009106214",
          "2025917",
          "2246552",
          "1000379039",
          "3013002167",
          "3000215273"
        ]
      }
    }
  ]
}