{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Pomona",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66930",
      "recalling_firm": "C.L.R. Medicals International, Inc.",
      "address_1": "748 E Bonita Ave Ste 210",
      "address_2": "N/A",
      "postal_code": "91767-1922",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and  Internationally to Egypt, Mexico, and Canada.",
      "recall_number": "Z-0531-2014",
      "product_description": "Viscocel and Viscocel Plus.    These products are intraocular fluid devices consisting of non-gaseous fluid intended to be introduced into the eye to aid performance of surgery, such as to maintain anterior chamber depth, preserve tissue integrity, protect tissue from surgical trauma, or function as a tamponade during retinal reattachment.",
      "product_quantity": "249,592 units",
      "reason_for_recall": "CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspection findings of deficiencies in the Quality System Regulations for Medical Device Manufacturers, 21 Code of Federal Regulation (CFR) Part 820 and lack of Premarket Approval (PMA) for devices sold or distributed in domestic commerce.  The Viscoelastic products, intended for human",
      "recall_initiation_date": "20131125",
      "center_classification_date": "20131220",
      "termination_date": "20141205",
      "report_date": "20140101",
      "code_info": "All lots manufactured September 01, 2011 to September 19, 2013.",
      "more_code_info": ""
    }
  ]
}