{
  "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": [
    {
      "status": "Terminated",
      "city": "Costa Mesa",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73386",
      "recalling_firm": "Innovative Ophthalmic Products, Inc",
      "address_1": "3184 Airway Ave Ste B",
      "address_2": "N/A",
      "postal_code": "92626-4619",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-1252-2016",
      "product_description": "Molteno3 Glaucoma Implants G-Series:    GS-Single Plate 175mm2 (IOP reorder#: M3-175)  GL-Single Plate 230mm2 (IOP reorder#: M3-230)",
      "product_quantity": "278 units",
      "reason_for_recall": "Innovative Ophthalmic Products (IOP) is recalling the Molteno 3 G-Series Glaucoma Implant the package insert/Instructions for Use (IFU) for the device has been updated to add a caution statement to minimize off-label use.",
      "recall_initiation_date": "20160222",
      "center_classification_date": "20160325",
      "termination_date": "20160916",
      "report_date": "20160406",
      "code_info": "GS2014  GL2014  GL2015  GS2015"
    }
  ]
}