{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Monrovia",
      "address_1": "1911 Walker Ave",
      "reason_for_recall": "The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).",
      "address_2": "",
      "product_quantity": "2,612 units",
      "code_info": "1281706, 1282812",
      "center_classification_date": "20160614",
      "distribution_pattern": "US",
      "state": "CA",
      "product_description": "STAAR AQ Cartridge-FP,  guide and delivery system for Intraocular lenses.",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Staar Surgical Co.",
      "recall_number": "Z-1964-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74067",
      "termination_date": "20161115",
      "more_code_info": "",
      "recall_initiation_date": "20160502",
      "postal_code": "91016-4846",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}