{
  "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-2539-2016",
      "product_description": "TRYX Antibacterial Envelope Rx Only    Product Usage:  Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)",
      "product_quantity": "3460 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   CMRM3122    lot number     15F30614  15F30614-A  15H10630  15K29659  16B05695    model number CMRM3133    lot number     15F18607  15G14620  15J29647  16C03706"
    }
  ]
}