{
  "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": "2026-07-08",
    "results": {
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    {
      "status": "Ongoing",
      "city": "Guaynabo",
      "state": "PR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96461",
      "recalling_firm": "Ethicon Endo Surgery,  LLC",
      "address_1": "475C - Suite 202",
      "address_2": "",
      "postal_code": "00969",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Germany, India, Israel, Japan, Lithuania, Mexico, Netherlands, New Zealand, Norway, Panama, Singapore, Spain, Taiwan, Uruguay.",
      "recall_number": "Z-1516-2025",
      "product_description": "ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH",
      "product_quantity": "2,556 units",
      "reason_for_recall": "Identified curing issues with the silicone during the needles manufacturing process.",
      "recall_initiation_date": "20250307",
      "center_classification_date": "20250403",
      "report_date": "20250409",
      "code_info": "Product Code: X843H-56; GMDN: 13906; UDI-DI: 10705031058088; Lot number: 10489X ;",
      "more_code_info": ""
    }
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}