{
  "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": "72 units",
      "code_info": "Lot numbers: M259970 and M267870",
      "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 Straight Fixed Extended Illuminated Laser Probe, Synergetics, length 7.5 ft, sterile / EO, 55.62.23P. 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-0882-2014",
      "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"
    }
  ]
}