{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Norcross",
      "address_1": "5550 Peachtree Pkwy Ste 500",
      "reason_for_recall": "Sterilization validation failure.",
      "address_2": "",
      "product_quantity": "956 units",
      "code_info": "Code: 131600, 131601, 131602, 131603, 131604, 131500, 131501, 131502, 131503, 131504 and 131506.",
      "center_classification_date": "20170518",
      "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.",
      "state": "GA",
      "product_description": "Brennen Skin Graft Mesher.    Surgical instrument designed to expand skin grafts'",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Molnlycke Health Care, Inc",
      "recall_number": "Z-2110-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77121",
      "more_code_info": "",
      "recall_initiation_date": "20170424",
      "postal_code": "30092-2555",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}