{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Oberdorf Bl",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85951",
      "recalling_firm": "Synthes Produktions GmbH",
      "address_1": "Eimattstrasse 3",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution including in the country of Australia, Germany, New Zealand, Slovakia, Spain, and Taiwan.",
      "recall_number": "Z-2739-2020",
      "product_description": "MatrixMIDFACE Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial skeleton in procedures such as craniotomies, reconstructive procedures, fracture repair, osteotomies, and selective orthognathic surgery of the maxilla and chin.",
      "product_quantity": "41 units",
      "reason_for_recall": "One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a  3  (representing 3mm) when it should have been packaged with body clip etched with a  12  (representing 12mm).",
      "recall_initiation_date": "20200616",
      "center_classification_date": "20200730",
      "termination_date": "20220415",
      "report_date": "20200805",
      "code_info": "Lot # 41P2340"
    }
  ]
}