{
  "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": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72997",
      "recalling_firm": "Rymed Technologies, LLC",
      "address_1": "6000 W William Cannon Dr Ste B300",
      "address_2": "N/A",
      "postal_code": "78749-1991",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution.",
      "recall_number": "Z-0676-2016",
      "product_description": "InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001.  Disposable, Single Use.     Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.",
      "product_quantity": "46,600 units",
      "reason_for_recall": "Potential for the female luer component of the InVision-Plus IV connector to crack during use.",
      "recall_initiation_date": "20160105",
      "center_classification_date": "20160121",
      "termination_date": "20161019",
      "report_date": "20160127",
      "code_info": "Catalog number RYM-7001 Lots: R01842, R01889, R01891, and R01897, Expire 03/2016.",
      "more_code_info": ""
    }
  ]
}