{
  "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": "Ongoing",
      "city": "San Daniele Del Friuli",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91869",
      "recalling_firm": "Limacorporate S.p.A",
      "address_1": "Via Nazionale 52",
      "address_2": "Di San Daniele",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: MO",
      "recall_number": "Z-1317-2023",
      "product_description": "SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210",
      "product_quantity": "1",
      "reason_for_recall": "Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct radiographic assessment of the hybrid glenoid position can be performed by the evaluation of the joint space, central TT peg position and cement mantel observation.",
      "recall_initiation_date": "20230221",
      "center_classification_date": "20230330",
      "report_date": "20230405",
      "code_info": "UDI-DI/Lot/Expiration: 08033390121798/2206565/2027-04-30"
    }
  ]
}