{
  "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": "Oak Creek",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83628",
      "recalling_firm": "Ad-Tech Medical Instrument Corporation",
      "address_1": "400 W Oakview Pkwy",
      "address_2": "N/A",
      "postal_code": "53154-7213",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY, PA, WI, AZ, IL, CA, NH, GA, MA, MN, UT, MI, WA, FL, TX, OH, OR, PA, MD, and India, Korea, Taiwan, Canada, Hong Kong, Denmark, Russia, Singapore, Japan, Brazil. UK, Spain, Czech Republic, France",
      "recall_number": "Z-2544-2019",
      "product_description": "AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits:  (a) REF DSG-90-2.3N  (b) REF DSG-6.3-090-2.4N",
      "product_quantity": "315 units",
      "reason_for_recall": "The inner diameter of the drill sleeve guide raw material was found to be under tolerance, potentially resulting in the drill bit seizing in the guide during surgery.",
      "recall_initiation_date": "20190827",
      "center_classification_date": "20190913",
      "termination_date": "20230405",
      "report_date": "20190925",
      "code_info": "All serial numbers distributed between January 2014 and May 2019"
    }
  ]
}