{
  "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": "2026-04-01",
    "results": {
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  "results": [
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      "status": "Ongoing",
      "city": "Deer Park",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96930",
      "recalling_firm": "Chamberlain Technologies LLC",
      "address_1": "21805 W Field Pkwy",
      "address_2": "N/A",
      "postal_code": "60010-3228",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to states of: Illinois, Nebraska, & California",
      "recall_number": "Z-1985-2025",
      "product_description": "SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030",
      "product_quantity": "10 units",
      "reason_for_recall": "Potential presence of residual adhesive material on the mesh surface.",
      "recall_initiation_date": "20220812",
      "center_classification_date": "20250617",
      "report_date": "20250625",
      "code_info": "Lot Code: Reference Number: Tintra E-3030 UDI: (01)00850011929063(17)250701(10)Z2459757G Lot Number: Z2459757G Expiration Date: 2025-07-01",
      "more_code_info": ""
    }
  ]
}