{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "O Fallon",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74918",
      "recalling_firm": "Synergetics Inc",
      "address_1": "3845 Corporate Centre Dr",
      "address_2": "N/A",
      "postal_code": "63368-8678",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Devices were distributed to KY, VA, TN, OH, IN, CA, NJ, NY, TX, SC, AL, MS, MI, and UT.  Foreign distribution to the UK, France, Mexico, and India.",
      "recall_number": "Z-0122-2017",
      "product_description": "25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in a Tyvek/Mylar double pouch configuration.",
      "product_quantity": "9 units",
      "reason_for_recall": "Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.",
      "recall_initiation_date": "20160811",
      "center_classification_date": "20161018",
      "termination_date": "20170427",
      "report_date": "20161026",
      "code_info": "Lot number M546500 (1 each or box of 6 each), exp 10/2018"
    }
  ]
}