{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salisbury",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90625",
      "recalling_firm": "Trinity Sterile,  Inc.",
      "address_1": "201 Kiley Dr",
      "address_2": "",
      "postal_code": "21801-2249",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of FL, PA.",
      "recall_number": "Z-1548-2022",
      "product_description": "Sklar Instruments IV Cath Dressing Tray Cs/25  Re-Order Number: 96-1708",
      "product_quantity": "5 cases (125 eaches )",
      "reason_for_recall": "Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy",
      "recall_initiation_date": "20220629",
      "center_classification_date": "20220818",
      "termination_date": "20240510",
      "report_date": "20220824",
      "code_info": "UDI-DI Number:  50649111317590 Case  10649111317590 Kit  Lot Numbers: 600001 600002",
      "more_code_info": ""
    }
  ]
}