{
  "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": "2026-09-23",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99707",
      "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 in the states of AL, AZ, CA, CO, FL, GA, IL, KS, LA, MA, MI, MO, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TX, VA, WI;",
      "recall_number": "Z-3173-2026",
      "product_description": "GM Helix Implant, REF: 109.984;",
      "product_quantity": "216",
      "reason_for_recall": "There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.",
      "recall_initiation_date": "20260812",
      "center_classification_date": "20260915",
      "report_date": "20260923",
      "code_info": "REF: 109.984; UDI: (01)7899878024552(11)251122(17)301121(10)VZPF4; Lot: VZPF4;",
      "more_code_info": ""
    }
  ]
}