{
  "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": "79751",
      "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": "USA (nationwide) Distribution",
      "recall_number": "Z-1526-2018",
      "product_description": "Hinge Coupling Hoffmann LRF Catalog # 4933-0-800    Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.",
      "product_quantity": "18",
      "reason_for_recall": "The wrong parts were picked for packaging. The connecting Nuts were  packed in the packaging labeled with Hinge coupling",
      "recall_initiation_date": "20180312",
      "center_classification_date": "20180426",
      "termination_date": "20200521",
      "report_date": "20180502",
      "code_info": "Lot # L23745"
    }
  ]
}