{
  "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": "Monmouth Junction",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74672",
      "recalling_firm": "TYRX Inc.",
      "address_1": "1 Deerpark Dr Ste G",
      "address_2": "N/A",
      "postal_code": "08852-1920",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2540-2016",
      "product_description": "TRYX Absorbable Antibacterial Envelope    Product Usage:  Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)",
      "product_quantity": "2993 units",
      "reason_for_recall": "TRYX products are being recalled since the processes of  spaying, welding, drying oven and polymer were not adequately validated.",
      "recall_initiation_date": "20160629",
      "center_classification_date": "20160815",
      "termination_date": "20171212",
      "report_date": "20160824",
      "code_info": "model number   CMRM6122     lot number  16E03727  16E05728    model number   CMRM6133    lot number   16E02726  16E06729"
    }
  ]
}