{
  "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": "175826",
      "product_res_number": "Z-0609-2020",
      "event_date_initiated": "2018-08-14",
      "event_date_created": "2019-12-05",
      "recall_status": "Completed",
      "res_event_number": "83595",
      "product_code": "LPM",
      "pma_numbers": [
        "P010019"
      ],
      "product_description": "Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile.  The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.",
      "code_info": "Lot numbers 31248224, exp. 2021/06; 31251806, exp. 2021/07; 31252524, exp. 2021/07; 31202568, exp. 2020/09; 31247324, exp. 2021/06; 31255298, exp. 2021/08; 31231184, exp. 2021/03; 31257909, exp. 2021/08; 31247744, exp. 2021/06; 31240720, exp. 2021/04; 31252252, exp. 2021/07; 31251559, exp., 2021/07; 31243321, exp. 2021/05; 31259174, 2021/09; 31256939, exp. 2021/08; 31257917, exp. 2021/08; 31256939, exp. 2021/08; 31257917, exp. 2021/08; 31242179, exp. 2021/05; 31251806, exp. 2021/07; and 31252524, exp. 2021/07.",
      "firm_fei_number": "3011073835",
      "recalling_firm": "Lens.com",
      "address_1": "4730 S Fort Apache Rd Ste 300 4730 S Fort Apache Rd",
      "address_2": "Ste 300",
      "city": "Las Vegas",
      "state": "NV",
      "postal_code": "89147-7947",
      "additional_info_contact": "Ms. Helen Junge\n800-536-7266",
      "reason_for_recall": "The product may be counterfeit and could have microbial issues.",
      "root_cause_description": "Counterfeit",
      "action": "The recalling firm sent undated emails beginning approximately 8/14/2018 to approximately 23,444  consumers and/or associated websites informing them the product they have received may be imitation.",
      "product_quantity": "1,600/6-contact lens cartons",
      "distribution_pattern": "Due to HIPAA, the firm only provided a spreadsheet that contained the first name, last initial, and zip code of each customer who received email notification of the recall.  Out of the 23,444 unique names on this list (25,162 names were actually listed due to multiple consumer orders), the firm believes approximately 800 of them to have received potentially counterfeit product.\n\nThe recalling firm was requested to provide a consumer spreadsheet showing the name, shipping address, and email address but declined because they thought it would be a violation of HIPAA regulations.",
      "openfda": {
        "pma_number": [
          "P890012",
          "P820086",
          "P790020",
          "P000030",
          "N17752",
          "P880029",
          "P080011",
          "P890023",
          "P830047",
          "P890049",
          "N16895",
          "N17987",
          "N18033",
          "P850057",
          "P940013",
          "P040045",
          "P790010",
          "P850033",
          "P840044",
          "P780013",
          "P960039",
          "N17679",
          "P850079",
          "P890040",
          "P850058",
          "P780007",
          "P810005",
          "P850078",
          "P220007",
          "P850077",
          "P850039",
          "P830037",
          "P990085",
          "P960022",
          "P010019",
          "P880098",
          "P850068",
          "P980006",
          "P840031",
          "P850072",
          "P780010",
          "P990072",
          "P170035",
          "P820021",
          "P860040"
        ],
        "registration_number": [
          "1123818",
          "3011771819",
          "3012138439",
          "3010890435",
          "3006015326",
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          "3007064560",
          "2919245",
          "3005724763",
          "3011649033",
          "3015332516",
          "3003365815",
          "2640128",
          "3044853379",
          "3014289638",
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          "9610813",
          "3017889743",
          "1053053",
          "3008586477",
          "9617710",
          "1314956"
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        "fei_number": [
          "3011771819",
          "3012138439",
          "3010890435",
          "3006015326",
          "3008504746",
          "3030421258",
          "3012167421",
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          "3015430860",
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          "3005939549",
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          "3003083595",
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          "1000222023",
          "1000305478",
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          "3006514242",
          "3002911336",
          "3003495738",
          "3007064560",
          "2919245",
          "3005724763",
          "3011649033",
          "3015332516",
          "3003365815",
          "3044853379",
          "1317628",
          "3014289638",
          "3010640396",
          "3006466212",
          "3030261726",
          "3002296055",
          "3017889743",
          "1053053",
          "3008586477",
          "3002806704",
          "1314956"
        ],
        "device_name": "Lenses, Soft Contact, Extended Wear",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.5925",
        "device_class": "3"
      }
    }
  ]
}