{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dallas",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93729",
      "recalling_firm": "FX SHOULDER",
      "address_1": "13465 Midway Rd Ste 310",
      "address_2": "",
      "postal_code": "75244-5183",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the state of NJ.",
      "recall_number": "Z-0843-2024",
      "product_description": "Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210",
      "product_quantity": "4",
      "reason_for_recall": "Centered glenosphere box may contain an eccentric glenosphere.",
      "recall_initiation_date": "20230808",
      "center_classification_date": "20240129",
      "report_date": "20240207",
      "code_info": "UDI-DI: 03701037309551, Lot: U0191",
      "more_code_info": ""
    }
  ]
}