{
  "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": [
    {
      "country": "United States",
      "city": "Sacramento",
      "address_1": "21 Goldenland Court Ste 100",
      "reason_for_recall": "Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the wrong thread direction.",
      "address_2": "",
      "product_quantity": "35 cases (10 each)",
      "code_info": "Model PTE 5002;  Lot number/ expiry date:  1424 PTE,  2019-04-24;  1428 PTE ,  2019-05-06;  1436 PTE, , 2019-06-16;  1440 PTE ,  2019-06-30;",
      "center_classification_date": "20170513",
      "distribution_pattern": "CA, MS, FL",
      "state": "CA",
      "product_description": "VORTRAN Automatic Resuscitator, VARPlus;  Model PTE-5002; Qty: 10 each    Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, constant flow, pressure cycled ventilatory  support.",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vortran Medical Technology 1, Inc",
      "recall_number": "Z-2091-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77072",
      "termination_date": "20171017",
      "more_code_info": "",
      "recall_initiation_date": "20170420",
      "postal_code": "95834-2427",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}