{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98265",
      "recalling_firm": "Straumann USA LLC",
      "address_1": "60 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1008",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1337-2026",
      "product_description": "WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM",
      "product_quantity": "561 units",
      "reason_for_recall": "The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.",
      "recall_initiation_date": "20260106",
      "center_classification_date": "20260209",
      "report_date": "20260218",
      "code_info": "Article Number: 065.4810; UDI-DI: 07630031741110; Lot numbers: VWPX4, VWPX6;"
    }
  ]
}