{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Austin",
      "address_1": "9800 Metric Blvd",
      "reason_for_recall": "It was discovered during a surgery that the design of the radius at the base of the pegs of the Anatomic Glenoid Trial (Part Numbers: 804-07-380, 804-07-420, 804-07-460, 804-07-500, and 804-07-540) is much larger on the trails than on the implants",
      "address_2": "",
      "product_quantity": "92 units",
      "code_info": "All Serial Numbers",
      "center_classification_date": "20180328",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "TX",
      "product_description": "Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 42mm, REF 804-07-420    Product Usage:  The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Encore Medical, Lp",
      "recall_number": "Z-1257-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79241",
      "more_code_info": "",
      "recall_initiation_date": "20180129",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Completed"
    }
  ]
}