{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Tucson",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92930",
      "recalling_firm": "SynCardia Systems LLC",
      "address_1": "1992 E Silverlake Rd",
      "address_2": "N/A",
      "postal_code": "85713-3865",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: FL, WI, AZ, TX, CA, OH, NC, IN, OK, IL, VA, NY, NE, PA, WA,  OUS: Saudi Arabia, Austria, Italy, Macedonia, Turkey, Germany,  France, Kuwait, Serbia, United Kingdom, Canada, Lithuania, Slovenia Australia",
      "recall_number": "Z-0126-2024",
      "product_description": "SynCardia 50cc TAH-t, Clinical, REF 570500, Sterile EO",
      "product_quantity": "114 units",
      "reason_for_recall": "Artificial hearts contain a epoxy resin that has not been reviewed by the FDA for safety and efficacy.",
      "recall_initiation_date": "20230801",
      "center_classification_date": "20231020",
      "report_date": "20231101",
      "code_info": "All Lots/ UDI: 00858000003053"
    }
  ]
}