{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "32694",
      "product_res_number": "Z-0857-04",
      "event_date_initiated": "2004-03-29",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-12-28",
      "res_event_number": "28667",
      "product_code": "MDV",
      "pma_numbers": [
        "P900052"
      ],
      "product_description": "Port-A-Cath II Epidural Low Profile Polysulfone/Titanium Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 5mm I.D., REF 21-1501-22",
      "code_info": "Lot M27037",
      "firm_fei_number": "2183502",
      "recalling_firm": "Deltec, Inc",
      "address_1": "1265 Grey Fox Rd",
      "city": "Saint Paul",
      "state": "MN",
      "postal_code": "55112-6929",
      "additional_info_contact": "Mike Herbert\t\n651-628-7049",
      "reason_for_recall": "Some of the outer product pouches have voids in the  seals and do not assure that the outer surfaces of the inner tray containing the port, catheter and procedural components remain sterile after sterilization.",
      "root_cause_description": "Other",
      "action": "A recall letter dated March 26, 2004 gave customers the option of returning the products or using the products if the customer's procedures do not require sterility of the outer surface of the inner tray.",
      "distribution_pattern": "The recalled products were shipped nationwide in the United States and worldwide.",
      "openfda": {}
    }
  ]
}