{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90074",
      "recalling_firm": "Medacta Usa Inc",
      "address_1": "3973 Delp St",
      "address_2": "",
      "postal_code": "38118-6110",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution was made to AK, CA, CT, IN, MA, NJ, and PA.  There was no foreign/military/government distribution.",
      "recall_number": "Z-1247-2022",
      "product_description": "GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1",
      "product_quantity": "50 units",
      "reason_for_recall": "A Size 2 trial baseplate was assembled with Size 1 instrument sets.",
      "recall_initiation_date": "20220413",
      "center_classification_date": "20220607",
      "termination_date": "20231023",
      "report_date": "20220615",
      "code_info": "Model Number/Reference Code: 11.01041; UDI-DI: 07630971252509; Lot Numbers Lots: 2109258 (exp. 06/24/2026), 2111198 (exp. 10/04/2026), 2115530 (exp. 10/27/2026)",
      "more_code_info": ""
    }
  ]
}