{
  "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": "Morgan Hill",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93079",
      "recalling_firm": "North Coast Medical Inc",
      "address_1": "135 E Main Ave Ste 110",
      "address_2": "N/A",
      "postal_code": "95037-7522",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US: NC, CA, WI OUS: New Zealand, Australia,",
      "recall_number": "Z-0125-2024",
      "product_description": "Gladiator, Wrist & Thumb Orthosis,  Part Numbers: NC86650 (Small/Left), NC86651 (Small/Right), NC86652 (Medium/Left), NC86653 (Medium/Right), NC86654 (Large/Left), NC86655 (Large/Right), NC86656 (X-Large/Left), and NC86657 (X-Large/Right)",
      "product_quantity": "27 units",
      "reason_for_recall": "The thumb strap of the wrist and thumb orthosis may contain latex that is not declared in the product labeling.",
      "recall_initiation_date": "20230818",
      "center_classification_date": "20231019",
      "report_date": "20231025",
      "code_info": "All Model Numbers without a manufacturing date on label"
    }
  ]
}