{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "65421",
      "product_res_number": "Z-0277-2008",
      "event_date_initiated": "2007-09-28",
      "event_date_posted": "2007-12-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-04-16",
      "res_event_number": "45420",
      "product_code": "OAT",
      "k_numbers": [
        "K060062"
      ],
      "product_description": "Straumann Palatal Implant , 04.1 L 4.2 mm,\nArticle Number: 042.335S, Straumann USA., LLC, Andover, Massachusetts, 01810-1008",
      "code_info": "Lot Numbers: 1001, F3776, F4662, F6563, E7083",
      "firm_fei_number": "3004975279",
      "recalling_firm": "Straumann USA LLC",
      "address_1": "60 Minuteman Rd",
      "city": "Andover",
      "state": "MA",
      "postal_code": "01810-1008",
      "additional_info_contact": "Same\n800-448-8168",
      "reason_for_recall": "Sticking Transfer Piece:  The Transfer Piece which accompanies the Palatal Implant may get stuck during implant requiring removal by using mechanical force.",
      "root_cause_description": "Device Design",
      "action": "Straumann USA, LLC sent Urgent Device Recall letters, via FedFx on 9/28/07, requesting the return of all Straumann Palatal Implant, articles 042.335 with lot numbers 1001, FE3776, F4662, F6563, E7083, and article 042.336S lot number 1001.",
      "product_quantity": "58 units",
      "distribution_pattern": "Nationwide Distribution - USA including states  of AZ, CA, CO, ID, IL, IN, GA, KY, NH , MA, MD, MI, NM,  PA, TX, UT, VA, and WA.",
      "openfda": {
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        ],
        "device_name": "Implant, Endosseous, Orthodontic",
        "medical_specialty_description": "Dental",
        "regulation_number": "872.3640",
        "device_class": "2",
        "registration_number": [
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