{
  "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": "2026-06-24",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98681",
      "recalling_firm": "Straumann USA LLC",
      "address_1": "60 Minuteman Rd",
      "address_2": "",
      "postal_code": "01810-1008",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.",
      "recall_number": "Z-1994-2026",
      "product_description": "Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304.    Endosseous Dental Implant Abutments",
      "product_quantity": "5 units",
      "reason_for_recall": "Includes an incorrect screw seat interface.",
      "recall_initiation_date": "20260327",
      "center_classification_date": "20260429",
      "report_date": "20260506",
      "code_info": "Article 010.0304. UDI: (01)07630031779977(11)YYMMDD(10)XXXXX. Project Numbers: 28000US_00811_00_b00, 28000US_00811_01_b00, 28000US_00426_00_b00, 28000US_00449_00_b00, 28000US_01266_00_b00.",
      "more_code_info": ""
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}