{
  "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": "Ongoing",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83037",
      "recalling_firm": "Encore Medical, Lp",
      "address_1": "9800 Metric Blvd",
      "address_2": "N/A",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US ( MS, NY, MO, OK, UT, AZ)",
      "recall_number": "Z-2090-2019",
      "product_description": "Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.",
      "product_quantity": "21",
      "reason_for_recall": "Manufacturing error, the drill bit shaft is unable to  properly capture the drill bit pin. Failure of the drill bit  shaft to capture the drill bit pin could result in the drill bit coming loose which could result in a  delay in surgery or adverse patient reaction resulting in a revision surgery.",
      "recall_initiation_date": "20180919",
      "center_classification_date": "20190727",
      "report_date": "20190807",
      "code_info": "Lot # 262667L01"
    }
  ]
}