{
  "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": "10 units",
      "code_info": "Lot Numbers:  ZB130801",
      "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: 32-420322\tPhase 3 Femoral Drill Guide Medium",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1737-2019",
      "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"
    }
  ]
}