{
  "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": "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-1549-2022",
      "product_description": "Wolf-Pak Premium Dressing Kit with GuardVA Cs/30    Ref: DC5030LF",
      "product_quantity": "1,513 cases\t(45,390 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:  10850007185760 Case 00850007185763 Kit   Lot Numbers: 600000 600001 600002 600003 600004 600005 600006 600007 600008",
      "more_code_info": ""
    }
  ]
}