{
  "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": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension.",
      "address_2": "",
      "product_quantity": "28 devices",
      "code_info": "Model No. 150802: Lot No. 305330 (UDI (01)00880304240230(17)220506(10)305330), 305340 ((01)00880304240230(17)220506(10)305330), 305350 ((01)00880304240230(17)220517(10)305350), 356750 ((01)00880304240230(17)220523(10)356750).",
      "center_classification_date": "20180215",
      "distribution_pattern": "US Nationwide Distribution to IN, MO, NY, TX.",
      "state": "IN",
      "product_description": "AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802.    Product Usage:  For use in Total Knee Arthroplasty.",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0627-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79095",
      "termination_date": "20180809",
      "more_code_info": "",
      "recall_initiation_date": "20170825",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}