{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91951",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of China, Germany, Sweden, Norway, Netherlands, Greece, Switzerland, France",
      "recall_number": "Z-1461-2023",
      "product_description": "GEM NEUROTUBE, Absorbable Woven Polyglycolic Acid Mesh Tube, Product Codes:  a) 5311-01240-010, b) 5311-01240-012;   for peripheral nerve repair",
      "product_quantity": "169 units",
      "reason_for_recall": "The product is brittle and potentially crumbling upon handling or when being removed from its package.",
      "recall_initiation_date": "20230327",
      "center_classification_date": "20230425",
      "report_date": "20230503",
      "code_info": "a) 5311-01240-010, Lot Number 19012112, exp. 12/31/2023;  b) 5311-01240-012, Lot Number 19012112, exp. 12/31/2023"
    }
  ]
}