{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Clearwater",
      "address_1": "21 N Park Place Blvd",
      "reason_for_recall": "Cosmetic imperfections on the surface of some lenses.",
      "address_2": "",
      "product_quantity": "70,440 units",
      "code_info": "Model MX60E and specific lots of the following SKU's: MXUE0000, MXUE0100, MXUE0200, MXUE0300, MXUE0400, MXUE0500, MXUE0600, MXUE0700, MXUE0800, MXUE0900, MXUE1000, MXUE1050, MXUE1100, MXUE1150, MXUE1200, MXUE1250, MXUE1300, MXUE1350, MXUE1400, MXUE1450, MXUE1500, MXUE1550, MXUE1600, MXUE1650, MXUE1700, MXUE1750, MXUE1800, MXUE1850, MXUE1900, MXUE1950, MXUE2000, MXUE2050, MXUE2100, MXUE2150, MXUE2200, MXUE2250, MXUE2300, MXUE2350, MXUE2400, MXUE2450, MXUE2500, MXUE2550, MXUE2600, MXUE2650, MXUE2700, MXUE2750, MXUE2800, MXUE2850, MXUE2900, MXUE2950, MXUE3000, MXUE3100, MXUE3200, MXUE3300, and  MXUE3400.",
      "center_classification_date": "20181218",
      "distribution_pattern": "US Nationwide Distribution: AL, AR, AZ, CA,  CO, CT, FL, GA, HI, IA, ID, IL IN, KS, KY, la, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY.",
      "state": "FL",
      "product_description": "enVista One Piece Hydrophobic Acrylic Intraocular lens -     Is indicated for primary implantation for the visual correction of aphakia in adult patients in whom the cataractous lens has been removed. The lens is intended for placement in the capsular bag.",
      "report_date": "20181226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bausch & Lomb Surgical, Inc.",
      "recall_number": "Z-0628-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81600",
      "termination_date": "20191104",
      "more_code_info": "",
      "recall_initiation_date": "20181105",
      "postal_code": "33759-3917",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}