{
  "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": "1800 W Center St",
      "reason_for_recall": "Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.",
      "address_2": "",
      "product_quantity": "11 units",
      "code_info": "Lot Numbers:  ZB161102  ZB170201  ZB170301  ZB170401  ZB170901",
      "center_classification_date": "20190606",
      "distribution_pattern": "CA, IN, LA, NM, NY, TX, WI  Foreign: CANADA,  AUSTRALIA, JAPAN, NETHERLANDS",
      "state": "IN",
      "product_description": "Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide:  Item Number: \t32-420323 Phase 3 Femoral Drill Guide Large",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1738-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82818",
      "termination_date": "20200910",
      "more_code_info": "",
      "recall_initiation_date": "20190418",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}