{
  "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": "Wolfhalden",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65908",
      "recalling_firm": "Medicel Ag",
      "address_1": "Luchton 1262",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1984-2013",
      "product_description": "Product Name: nanoPOINT Injector System, item number 37-0000-08.    Intended to fold and insert a STAAR Surgical Collamer¿ nanoFLEX or Afinity IOLs, through surgical procedure in a human eye.",
      "product_quantity": "68 boxes or 680 units",
      "reason_for_recall": "The firm initiated this recall of one lot (121402) of nanoPOINT Injectors after they noticed that Tyvek lids might have been damaged and, therefore, the stability of the sterile barrier might be negatively affected.",
      "recall_initiation_date": "20130805",
      "center_classification_date": "20130820",
      "termination_date": "20140311",
      "report_date": "20130828",
      "code_info": "Item number 37-0000-08    Lot number of the recalled products: LOT121402"
    }
  ]
}