{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Daniele Del Friuli",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71972",
      "recalling_firm": "Limacorporate S.p.A",
      "address_1": "Via Nazionale 52",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of: OH, TX, NC, NY, CA, FL, KS, AL, MI, MT, CO, MO, NV, WA, MN and LA., and Internationally to Australia.",
      "recall_number": "Z-2540-2015",
      "product_description": "SMR Shoulder/Spalla Trial Heads ECC .4 mm Adaptor, REF 9013.30.021; SMR Shoulder/Spalla Trial Heads ECC .8 mm Adaptor, REF 9013.30.031;   for use in shoulder implant surgery.",
      "product_quantity": "93 units",
      "reason_for_recall": "The dimensions of the mating features of the recalled products are out of specification causing the device to be difficult to assemble.",
      "recall_initiation_date": "20150814",
      "center_classification_date": "20150902",
      "termination_date": "20160226",
      "report_date": "20150909",
      "code_info": "Lot Numbers: 14AA146 and 14AA153"
    }
  ]
}