{
  "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": "2026-08-22",
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      "product_res_number": "Z-0906-2022",
      "event_date_initiated": "2022-02-28",
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      "recall_status": "Open, Classified",
      "res_event_number": "89830",
      "product_code": "FXG",
      "product_description": "Integra Universal Flexible Arm part number REF 1362275",
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      "firm_fei_number": "3003418325",
      "recalling_firm": "Integra LifeSciences Corp.",
      "address_1": "1100 Campus Rd",
      "city": "Princeton",
      "state": "NJ",
      "postal_code": "08540-6650",
      "additional_info_contact": "609-275-0500",
      "reason_for_recall": "Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.",
      "root_cause_description": "Device Design",
      "action": "Urgent Voluntary Medical Device Recall Notice dated 02/28/2022 was sent via FexEx.  Customers are instructed to remove the affected product from service, return it to Integra and complete and submit the attached acknowledgment form.  Contact Customer Service with questions: Phone: 1-800-654-2873, Email: custsvcnj@integralife.com",
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