{
  "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": [
    {
      "status": "Terminated",
      "city": "Selzach",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80198",
      "recalling_firm": "Stryker GmbH",
      "address_1": "Bohnackerweg 1",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD & TX",
      "recall_number": "Z-2244-2018",
      "product_description": "Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463",
      "product_quantity": "18 parts (10 parts quarantined)",
      "reason_for_recall": "Laser etching which indicates whether the device is in   compression or distraction mode appears to be on the wrong side of the lever arm",
      "recall_initiation_date": "20180504",
      "center_classification_date": "20180615",
      "termination_date": "20200427",
      "report_date": "20180627",
      "code_info": "Lot # 04857V"
    }
  ]
}