{
  "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": [
    {
      "country": "United States",
      "city": "O Fallon",
      "address_1": "3845 Corporate Centre Dr",
      "reason_for_recall": "Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.",
      "address_2": "",
      "product_quantity": "102 Units",
      "code_info": "Lot numbers: M257130 and M265370",
      "center_classification_date": "20140130",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Argentina, Austria, Brazil, Canada, China, Egypt, France, Germany, Greece, Hong Kong, Italy, Japan, Mexico, Morocco, the Netherlands, Pakistan, South Korea, Spain, Sweden, Switzerland, and the United Kingdom.",
      "state": "MO",
      "product_description": "23ga Endo Illuminator (Eckardt Trocar Compatible), Synergetics, inc., length 8.0 ft, sterile / EO, 56.02.23P Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synergetics Inc",
      "recall_number": "Z-0884-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67147",
      "termination_date": "20150325",
      "more_code_info": "",
      "recall_initiation_date": "20131209",
      "postal_code": "63368-8678",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}