{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "31145",
      "product_res_number": "Z-0378-04",
      "event_date_initiated": "2004-01-06",
      "event_date_posted": "2004-01-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-01-04",
      "res_event_number": "28070",
      "product_code": "KYB",
      "product_description": "MicroSTAAR Injector Cartridges Models:\n\nSFC-25 (utilized with plate haptic Collamer lens)\nMTC-60 (utilized with plate haptic Silicone lens)",
      "code_info": "SFC-25 (8 lots) 1180608, 1181078, 1181170,1181171, 1181396, 1181397, 1182237, 1184864 MTC-60 (25 lots) 1177222, 1177950, 1178121, 1178212, 1176868, 1177421, 1178738, 1178883, 1178885, 1179023, 1181789, 1181790, 1181797, 1181798, 1181980, 1182245, 1182342, 1182343, 1182344, 1182345, 1182675, 1182676, 1182677, 1182761.",
      "firm_fei_number": "2023826",
      "recalling_firm": "Staar Surgical Co Inc",
      "address_1": "1911 Walker Ave",
      "city": "Monrovia",
      "state": "CA",
      "postal_code": "91016-4846",
      "additional_info_contact": "Jason K. Lyon\n626-303-7902 Ext. 2273",
      "reason_for_recall": "Increased numbers of lens tears during placement of lens into eye.",
      "root_cause_description": "Other",
      "action": "Customers will recieve recall notice, Customer Bulletin and MicroStaar Injector Cartridge Guide by Federal Espress (sent 1/6/04).",
      "distribution_pattern": "Nationwide, Canada and Australia",
      "openfda": {
        "k_number": [
          "K001157",
          "K832939",
          "K860148",
          "K821381",
          "K840694",
          "K871440",
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          "K954600",
          "K792066",
          "K940593",
          "K063694",
          "K854994",
          "K811718",
          "K032412",
          "K840104",
          "K930320",
          "K951292",
          "K883489",
          "K870265",
          "K823222",
          "K965185",
          "K152357",
          "K081382",
          "K903574",
          "K861085",
          "K791351",
          "K903575",
          "K983129",
          "K981571",
          "K861990",
          "K063155",
          "K070669",
          "K930628",
          "K072985",
          "K022723",
          "K941603",
          "K854197",
          "K970033",
          "K961242"
        ],
        "registration_number": [
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        ],
        "fei_number": [
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          "1119279",
          "3010208880",
          "3002681132",
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          "3010148516",
          "1000117501",
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          "3546",
          "3003951061",
          "1000138054",
          "1000114185",
          "1317628",
          "2023826",
          "3012236936",
          "1220477",
          "3006946276",
          "3003591781",
          "3017636737",
          "1000125771",
          "1000581837",
          "1000231766",
          "3009646326",
          "2648035",
          "3023657851"
        ],
        "device_name": "Lens, Guide, Intraocular",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.4300",
        "device_class": "1"
      }
    }
  ]
}