{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89321",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution in the states of FL, IL, OH",
      "recall_number": "Z-0513-2022",
      "product_description": "Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5  Article Number: 138.107",
      "product_quantity": "1 unit",
      "reason_for_recall": "Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 has an implant with measure of 3.5x13mm; and Carton Box (138.107- Easypack Helix GM Acqua has a 3.5x8mm implant instead of a 3.5x 13mm implant",
      "recall_initiation_date": "20211130",
      "center_classification_date": "20220119",
      "termination_date": "20250205",
      "report_date": "20220126",
      "code_info": "Lot GNV20:   UDI:7899878052906"
    }
  ]
}