{
  "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": "2026-09-05",
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      "recall_status": "Open, Classified",
      "res_event_number": "77121",
      "product_code": "FZW",
      "product_description": "Brennen Skin Graft Mesher.\n\nSurgical instrument designed to expand skin grafts'",
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      "firm_fei_number": "1629080",
      "recalling_firm": "Molnlycke Health Care, Inc",
      "address_1": "5550 Peachtree Pkwy Ste 500 5550 Peachtree Pkwy",
      "address_2": "Ste 500",
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      "state": "GA",
      "postal_code": "30092-2555",
      "additional_info_contact": "Angela L. Bunn\n470-375-0048",
      "reason_for_recall": "Sterilization validation failure.",
      "root_cause_description": "Process design",
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      "distribution_pattern": "Domestic: U.S. Nationwide; Foreign: Austria, Australia, Bangladesh, Canada, Chile, Germany, Denmark, Finland, France, Great Britain, Hong Kong, Hungary, Ireland, India, Italy, Jordan, Korea, Kuwait, Malaysia, Norway, New Zealand, Peru, Saudi Arabia, Sweden Switzerland, Taiwan, Turkey, South Africa, United Arab Emirates.",
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