{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Clearwater",
      "address_1": "21 N Park Place Blvd",
      "reason_for_recall": "Complaints concerning kinked haptics that were occurring during lens delivery.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Lot Number:  H671901 Expiration Date: Dec-17,   Lot Number:  H672001 Expiration Date: Nov-17,  Lot Number:  H672602 Expiration Date: Dec-17,  Lot Number:  H674001 Expiration Date: Dec-17,  Lot Number:  H674401 Expiration Date: Nov-17,  Lot Number:  H674801 Expiration Date: Dec-17,  Lot Number:  H675401 Expiration Date: Dec-17,  Lot Number:  H740301 Expiration Date: Dec-17, and   Lot Number:  H743201 Expiration Date: Feb-18.",
      "center_classification_date": "20170516",
      "distribution_pattern": "Nationwide Distribution to AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY, and Puerto Rico",
      "state": "FL",
      "product_description": "SoftPort Easy-Load Lens Delivery System  Model: EZ-28V  Is used for the folding and delivering of the LI61AO, LI61AOV, or LI61SE 3-piece lens into the eye. The SofPort Easy-Load Lens Delivery System consists of a syringe shaped body and tip with a plunger, drawer, and haptic puller. It is a sterile, disposable plastic device designed for single use only.",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bausch & Lomb Surgical, Inc.",
      "recall_number": "Z-2098-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77087",
      "termination_date": "20191211",
      "more_code_info": "",
      "recall_initiation_date": "20170405",
      "postal_code": "33759-3917",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}